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Videos uploaded by user “BioPharmSystems”
Preparing Clinical Trial Data for Reporting and Analysis
 
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Learn a better way to prepare clinical trial data for reporting and analysis. -- Many companies have made great strides in standardizing and conforming subject data collected in clinical trials, in order to have a more efficient and repeatable way of delivering the data to reporting systems for statistical analysis and regulatory submissions. Typically, preparing data is made up of the following three steps: 1. Specifying the conformed data 2. Programming the conformed specification 3. Validating the written programs work as expected Please join BioPharm Systems' Michael Grossman, vice president of clinical data warehousing and analytics, for a complimentary one-hour webinar that will discuss and demonstrate one way to dramatically reduce the effort of specification and validation, as well as remove the programming step in its entirety. The ensuing programs are automatically generated in Oracle Life Sciences Data Hub (LSH) and as standalone SAS. The end result is a significant increase in the productivity of data preparation and conforming for internal use, along with runnable programs that can be sent to regulatory authorities and partners. To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/sldl6locwp3e. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 28004 BioPharmSystems
Medical Coding with MedDRA
 
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Learn about the best practices for medical coding using MedDRA, a global dictionary used by companies for regulatory activities. -- MedDRA is a global dictionary used by companies for regulatory activities. The dictionary, complete with clinically validated terminology, is used to classify adverse event information related to the use of drugs, devices, and other therapies. Coding the data to a standard set of MedDRA terms enables health authorities and the life sciences industry to more readily exchange and analyze data. MedDRA is considered the international standard for adverse event classification. However, while the data volume and standardization capabilities offered by the dictionary can provide significant benefits, the multi-axial design and data specificity can introduce considerable challenges that could lead to the inaccurate classification of data. Join BioPharm Systems' Dr. Rodney Lemery, vice president of safety and pharmacovigilance, and Caroline Halsey, director of project management, EMEA, for this free one-hour webinar that will explore the best practices for medical coding using MedDRA. To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/fqfuit5ql7qh. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 15058 BioPharmSystems
What is a Clinical Trial Management System (CTMS)?
 
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Learn the basics of clinical trial management systems (CTMS). -- If you've ever wondered what a CTMS is, how one is beneficial, or how to select and implement one, then this webinar is for you. Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this one-hour session that will provide you with a basic understanding of clinical trial management systems. This webinar will answer the following questions: -What is a CTMS? -Which types of organizations need one? -How do you choose one? -How do you decide on an implementation strategy? -What are the best practices to consider for implementation? -What are some implementation pitfalls to avoid? To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/1s0dn4vwxki. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 14442 BioPharmSystems
Using Oracle's Argus Safety to Comply with ICH E2B(R3)
 
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Learn about the new Individual Case Safety Report (ICSR) international standard and upcoming ICSR reporting changes. -- The new ISO Individual Case Safety Report (ICSR) standard is being finalized in 2011. A major revision of the ICH E2B guideline is progressing based on the new ICSR standard with an ICH step 2 consultation of the ICH E2B(R3) Implementation Guide expected by the end of June 2011. An overview of the proposed changes to the ICSR Final Draft International Standard (FDIS) and its implementation will be discussed, along with the expected changes to the ICSR reporting in the context of the new European pharmacovigilance legislation. Join BioPharm Systems' Andrew Mitchell, EMEA safety and pharmacovigilance practice lead, for this one-hour presentation that will include: -- Discussion of the upcoming ISO Individual Case Safety Report (ICSR) standard known as ICH E2B(R3) -- Electronic reporting of ICSRs and EudraVigilance in the context of the new European pharmacovigilance legislation -- Using Argus Safety to comply with the information and regulations above and how this affects your upgrade planning To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/f9da1w6pjn8f. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 20914 BioPharmSystems
Overview of Simple Forms EDC (used with Oracle Clinical)
 
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Learn about Simple Forms, an electronic data capture (EDC) system and survey tool that can be used with Oracle Clinical. -- Simple Forms, a low-cost and intuitive EDC system, has been implemented at biopharmaceutical, medical device, and contract research organizations since 2005. The solution is designed to be used with Oracle Clinical, with or without Remote Data Capture (RDC). Some of the features and benefits: • Due to the simplicity of the system, no training is required • Choose from 5 languages with a click of a button (English, French, German, Italian, and Spanish) • E-mail specific users upon submission of a form to help keep data entry on track • Collect survey data • No plug-ins required • No 3rd party software required, aside from Oracle Clinical • Use with any operating system and browser Join Michelle Engler, the chief architect of Simple Forms, for a one-hour presentation that will include a live demonstration of this EDC solution. If you prefer a private demonstration at your convenience, please let us know at [email protected] To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/7rfge8xuqqte. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 19664 BioPharmSystems
Integrating Siebel Clinical with Oracle Clinical and Remote Data Capture
 
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Param Singh, Vice President of Clinical Trial Management Solutions, discusses integrating a custom configuration of Siebel CTMS with Oracle Clinical and Remote Data Capture. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 1138 BioPharmSystems
Argus Safety | Streamlining Drug Safety and Pharmacovigilance Operations
 
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Learn about a major pharmaceutical company's pharmacovigilance globalization initiative that helped standardize and streamline its operations. -- As the focus on international product safety regulations increases, life sciences organizations must globalize and enhance their safety and pharmacovigilance operations in order to successfully navigate through the challenges they are presented with. Join BioPharm Systems' Dr. Rodney Lemery, vice president of safety and pharmacovigilance, for this free one-hour webinar that will discuss a major pharmaceutical company's pharmacovigilance globalization initiative that helped standardize and streamline its operations. Several topics that will be discussed include: -- SOP Integration -- Standardization of Local Practices -- Departmental Coordination -- Varying Reporting Requirements To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/5fvklbeknq9q. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 8524 BioPharmSystems
Argus Safety Overview
 
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Oracle's Argus Safety is a comprehensive and industry-proven system designed specifically to address the life sciences industry's complex drug safety and pharmacovigilance requirements. Visit http://www.biopharm.com for a demonstration or simply to learn more about BioPharm's Argus Safety implementation, migration, private cloud hosting, and training services. We have an experienced team that can help you install and manage all of the database's modules, including Argus Safety Japan.
Views: 4146 BioPharmSystems
BioPharm Systems in 139 Seconds
 
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BioPharm Systems (http://www.biopharm.com) is an IT consulting company that focuses on the life sciences industry. We have extensive experience in the implementation, integration, migration, and hosting of the following Oracle clinical trial management, drug safety and pharmacovigilance, clinical data warehousing and analytics, clinical data management, and electronic data capture systems: -Siebel Clinical -Argus Safety Suite (Argus Safety, Affiliate, Interchange, Dossier, Insight, and Perceptive) -Adverse Event Reporting System (AERS) -Empirica Signal and Empirica Topics -Life Sciences Data Hub (LSH) -Clinical Development Analytics (CDA) -Oracle Clinical -Remote Data Capture (RDC) -Thesaurus Management System (TMS) Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 4204 BioPharmSystems
Study Design/Setup in Oracle Clinical and Remote Data Capture (RDC)
 
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Learn about the flexible study design features in Oracle Clinical and Remote Data Capture (RDC). -- Oracle Clinical (OC) / Remote Data Capture (RDC) 4.6 provides the ability to conduct global clinical trials more efficiently and effectively. The newest release features significant enhancements that enable and support complex study design scenarios. Increasing the efficiency of clinical trials, the application enables sponsors and CROs to dynamically drive patient visits and assessment schedules based on subject data and clinical outcomes, boosting the productivity and the effectiveness of a clinical trial. Join BioPharm Systems' chief application expert, Steve Rifkin, for this free one-hour webinar to examine the new flexible study design features in the latest version of OC/RDC. This webinar will include both a discussion and demonstration of OC/RDC product features. To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/snmsyp0sil8n. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 10617 BioPharmSystems
Siebel Clinical Trial Management System Implementations
 
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Learn about Oracle Siebel CTMS implementations. -- Implementing Siebel Clinical, Oracle's clinical trial management system (CTMS) doesn't have to take very long or be difficult. Watch this video to learn about BioPharm's unique CTMS implementation methods. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/+BioPharm
Views: 1193 BioPharmSystems
Oracle Life Sciences Data Hub (LSH) Implementation
 
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Learn the best way to implement and configure Life Sciences Data Hub, Oracle's clinical data warehouse. -- BioPharm Systems has implemented Oracle Life Sciences Data Hub (LSH) on-site and as a hosted solution for numerous sponsors and clinical research organizations (CROs). As a result, the company has established many best practices for implementing LSH to support clinical data submissions and the pooling of data across studies and projects that require special purpose reporting and analytics. Please join BioPharm Systems' Mike Grossman, vice president of clinical data warehousing and analytics, for this complimentary 60-minute webinar in which he will discuss the best way to implement and configure the clinical data warehouse, so that the solution enables complete cross-study, cross-compound analysis and reporting, as well as the creation of an analytics strategy. To view this webinar in its entirety, please visit: https://cc.readytalk.com/r/3zj046psguun&eom Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 3463 BioPharmSystems
Using Oracle's Data Management Workbench (DMW) with InForm and Other Sources
 
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Learn how Oracle Health Sciences Data Management Workbench (DMW) can be used to optimize the management of clinical data from InForm and other sources. -- Data Management Workbench (DMW), an application that was recently introduced as part of Oracle's life sciences data warehousing suite, is designed to combine data from various clinical data sources, such as InForm, and transform it into standard data models. In addition to the many features DMW offers, the solution enables you to run cross-data source edit checks and perform data reviews. Please join BioPharm's Mike Grossman, vice president of clinical data warehousing and analytics, for this complimentary 60-minute webinar in which he will demonstrate how DMW loads, transforms, and cleans trial data from InForm 6.0 and a central lab. He will also show how to use the data for downstream reporting and analysis. To view this webinar in its entirety, please visit: https://cc.readytalk.com/r/xzgb9ola6ji1&eom. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/+BioPharm
Views: 4066 BioPharmSystems
Automating Site Payments in Siebel Clinical
 
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Learn about automating your clinical/site payments in Siebel Clinical. -- BioPharm can integrate your EDC system with Siebel Clinical so that patient information, such as completion dates for each visit and procedure, is automatically populated. Then you can generate a payment request in Siebel Clinical that is automatically sent to your finance group through another integration. As soon as finance processes that payment request in their system, the integration sends the payment details back to the clinical trial management system (CTMS). Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/+BioPharm
Views: 182 BioPharmSystems
ClearTrial - Clinical Trial Budgeting Software
 
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Learn about ClearTrial, Oracle's clinical study budgeting software. ClearTrial is a subscription-based, cloud system that enables sponsors and clinical research organizations (CROs) to quickly and accurately develop budgets and timelines for clinical studies. To learn more about BioPharm Systems and our ClearTrial services, visit www.biopharm.com.
Views: 1421 BioPharmSystems
Why You Need a Clinical Trial Management System (CTMS)
 
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Learn about the top 10 reasons why it makes sense for organizations to invest in a clinical trial management system (CTMS). -- Trying to build a business case for a clinical trial management system (CTMS) at your organization? Let us help you! BioPharm Systems' Clinical Trial Management Solutions practice has decades of experience with CTMS implementations for organizations of all sizes. Over the years, our clients have told us the ways in which having a CTMS has benefited them, and we would like to pass the top ten on to you. Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this free one-hour webinar in which he breaks down each of the top ten reasons why it makes sense for organizations to invest in a CTMS. A live demonstration of the two most popular reasons and corresponding features (voted on by attendees during webinar) will be performed. To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/cr589b5wgl3l. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 3784 BioPharmSystems
Clinical Trial Management System (CTMS) and Electronic Document Management System (EDMS) Integration
 
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Learn why you should integrate your clinical trial management system (CTMS) and document management system (EDMS), as well as two approaches to integrating the systems. -- Virtually every CTMS, such as Siebel Clinical/ASCEND, includes some form of document tracking functionality. Now, imagine if you could share information about the documents tracked in your CTMS with your EDMS, and even transfer stored files between the two systems. A CTMS and EDMS integration could significantly streamline your clinical document tracking process and help keep you in compliance. Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this free one-hour presentation that will explore two approaches to integrating your CTMS with your EDMS. A live demonstration of a CTMS and EDMS integration approach will be performed. To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/1ru4l89e1bkm. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 4628 BioPharmSystems
Oracle Clinical / Remote Data Capture (RDC) 4.6 Features
 
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Learn about several features in Oracle Clinical and Remote Data Capture (RDC).-- Implementation of Oracle Clinical (OC) and Remote Data Capture (RDC) 4.6 provides life sciences organizations with more options for designing clinical trials. This most recent version of OC/RDC offers features that support adaptive trials and provide ease of use for the end user, while better securing a sponsor's data. Join BioPharm Systems' Principal Consultant, Mari Clovis, for this one-hour session to learn about these new features and other updates: -Defining conditional logic within forms -Using flexible study options for adaptive trials -Restricting access to selected forms -Hiding and preventing updates to queries based on user roles -Miscellaneous updates To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/5t2q59ufjbpx. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 3899 BioPharmSystems
Oracle Siebel CTMS Open UI Overview
 
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Learn more about Siebel CTMS Open UI, the newest release of Oracle's clinical trial management system. -- Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/+BioPharm
Views: 484 BioPharmSystems
Integrating Oracle Argus Safety with Clinical Systems Using Argus Interchange E2B Functionality
 
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Learn about integrating Oracle's Argus Safety with other clinical systems using Argus Interchange's E2B capabilities. -- Over the past few years, companies conducting clinical trials have increasingly been interested in integrating their pharmacovigilance systems with other clinical and safety solutions to streamline their processes. Please join BioPharm Systems' Dr. Rodney Lemery, vice president of safety and pharmacovigilance, for a one-hour webinar in which he will discuss the ability to integrate Oracle's Argus Safety with other applications using the safety system's inherent extended E2B functionality. This presentation will cover two Argus Safety integration projects - one that has been completed and one that is ongoing. The discussion will include the conceptual framework for these integration bridges and will identify issues, concerns, and their respective mitigation strategies. After attending this tutorial, you will have an increased understanding of Argus' extended E2B capabilities and the typical points of discussion for similar projects. To view this webinar in its entirety, please visit: https://cc.readytalk.com/r/x4mjn5dm2r06&eom Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/+BioPharm
Views: 1760 BioPharmSystems
How Oracle Argus Safety Migrations Work
 
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Learn how to migrate to Oracle's Argus Safety. -- Is your organization considering migrating to Argus Safety, Oracle's comprehensive safety and pharmacovigilance system? Then you probably already know that moving and reformatting legacy adverse event cases can be a major bottleneck. BioPharm, with our partner, Valiance, can quickly automate and streamline many aspects of the migration and implementation process without resorting to custom scripts, existing APIs, and time-consuming manual tasks. From the assessment and strategy to the complete migration and verification of adverse event cases from your source system (e.g., AERS, ARISg, Excel, Trace, Custom, etc.), leveraging our tried-and-true methodologies and technologies helps you accelerate the entire process with confidence. Please join BioPharm's Dr. Rodney Lemery and Valiance's Richard Wells for a free one-hour webinar that will explore: -- The types of risks and challenges associated with safety data system migrations, including those related to Japan and other countries -- How to successfully approach a safety and pharmacovigilance system migration and implementation project -- The benefits of pre-configured migration software and automated 100% migration testing -- Examples of past migration and implementation projects -- Your own migration questions and challenges To view this webinar in its entirety, please visit: https://cc.readytalk.com/r/c281688i2iki&eom Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/+BioPharm
Views: 1761 BioPharmSystems
Clinical Trial Management System (CTMS) Data Migration
 
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Learn how the data in an existing clinical trial management system (CTMS) should be handled when migrating to a new application. -- You are considering implementing a new clinical trial management system (CTMS), or maybe you have already made the decision. But you are wondering: What should we do with the data in our legacy system? Is it worth migrating? Should we migrate all of the data or just some of it? When should we migrate? What methods should we use? Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this complimentary one-hour session that will: -Explore all facets of data migration -Offer guidance applicable to any organization -Include a live demonstration of ASCEND-Migrate, a data migration tool designed to streamline the migration from any investigator database to Oracle's Siebel Clinical application To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/adzlsog8cgxk. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 1226 BioPharmSystems
Siebel Clinical (CTMS) iHelp Overview
 
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Learn more about iHelp, an interactive and context-sensitive user documentation system that comes with Siebel CTMS. -- Have you ever found yourself stuck on a task in Siebel Clinical, Oracle's Clinical Trial Management System (CTMS)? Or, have your organization's users ever complained about forgetting how to perform a task? Although you may already have a comprehensive user guide, it's probably quite lengthy (perhaps over 300 pages!) and cumbersome to use. Wouldn't it be nice if Siebel Clinical had a guide built right into the application that could provide step-by-step instructions and tips exactly when and where you need them? Enter iHelp. iHelp is an interactive and context-sensitive user documentation system that comes with Siebel Clinical. That's right -- if you have Siebel Clinical, you already have iHelp. From quick pointers to full sets of instructions, iHelp can guide you through the steps in real-time. The level of detail is entirely up to you -- each organization has the power to create iHelp content that is 100% relevant to their users' needs. No more getting stuck! Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, and Richard Gavan, CTMS consultant, for this free one-hour webinar and demonstration in which they will: -- Provide a general overview of iHelp -- Discuss ways companies like yours are currently using the feature -- Share useful methods of deploying iHelp content -- Explain the basics of iHelp administration and development Training one or two users to develop content in iHelp could help the rest of your users become experts in Siebel Clinical, minimizing your need for refresher training, reference materials, and user support. Register to learn more! To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/k5zuw3g6ybuy. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 2734 BioPharmSystems
Managing Global Studies with Oracle's Siebel CTMS
 
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Learn several ways in which Oracle's Siebel CTMS can help sponsors, CROs, and AROs, ease the complexities of managing global studies. -- While clinical trials are increasingly being carried out in multiple countries, organizations that run these global clinical trials are faced with a number of challenges, such as: -- Adhering to varying regulatory requirements -- Dealing with multiple currencies for payments -- Selecting and managing vendors in various countries -- Working in areas with less sophisticated infrastructures Join us for this free one-hour webinar in which Param Singh, vice president of clinical trial management solutions, BioPharm Systems, will discuss several ways in which Oracle's Siebel CTMS can help sponsors, CROs, and AROs, ease the complexities of managing global studies. The webinar will include case studies of current BioPharm clients, as well as live demonstrations of key functionality. To view this webinar in its entirety, please visit: https://cc.readytalk.com/r/e91w0m8wtbpl&eom. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 2379 BioPharmSystems
Mitigating Risks with Clinical and Safety/Pharmacovigilance Systems
 
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Learn the business risks related to clinical and safety systems and how the risks inherent in implementing complex CTMS and safety systems can be significantly reduced. -- All business processes are subject to some level of risk. Key to the long term viability of any company is the critical need to identify the risks, quantify them, minimize them, and have a clear plan for dealing with any residual risks. Organizations try to mitigate risks by implementing systems that support the company's business processes. Commercial software systems that are available from vendors such as Oracle include many capabilities which, if implemented properly, greatly reduce the risks in the business process. The implementation of complex systems is, in itself, a risky process. Organizations like BioPharm Systems have been able to use their wide range of experience to develop pre-configured and pre-validated solutions that help reduce the risks during the implementation of a clinical trial management system (CTMS) and a safety system. This one and a half-hour webinar will provide an overview of business risks related to clinical and safety systems and will illustrate how the risks inherent in implementing complex CTMS and safety systems can be significantly reduced. To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/a5ve1gnyspsq. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 2752 BioPharmSystems
Evaluating and Investigating Drug Safety Signals with Public Databases
 
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Learn about several public databases available to use during the evaluation of safety signals. -- In this one-hour webinar, BioPharm Systems' Dr. Rodney Lemery, vice president of safety and pharmacovigilance, will review a number of public databases available to use during the evaluation and investigation of identified safety signals. The discussion will focus on the use of free and paid longitudinal healthcare databases available online. After attending this presentation, you will better understand how these data sources can be used in your daily PV work. Agenda Highlights: -- Overview of signal management -- Overview of epidemiology -- Review of free and paid databases To view this webinar in its entirety, please visit: https://cc.readytalk.com/r/eagsm4a1unid&eom Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/+BioPharm
Views: 1354 BioPharmSystems
Oracle Argus Safety and Argus Safety Japan Benefits
 
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Learn how Argus Safety and Argus Safety Japan help you to meet challenges by providing a single global database and integrated workflow process for superior safety reporting capabilities -- Achieving complete and efficient reporting of adverse drug reactions is a critical goal for all companies involved in developing and delivering medicinal products to the world's population. These companies include pharmaceutical, biotech, medical device, contract research organizations (CROs), charitable and not-for-profit organizations and academic institutions. While the challenge of efficient and effective safety reporting to two of the major regulatory agencies -- FDA and EMA -- is substantial, the additional challenge of reporting to the Japanese regulatory authority, the PMDA, in a way that integrates with an existing safety reporting process and function is significantly greater. Argus Safety and Argus Safety Japan together help you to meet these challenges by providing a single global database and integrated workflow process for superior safety reporting capabilities. This webinar will be of interest and relevance to all organizations that need a robust and proven safety system to meet their global regulatory reporting requirements. It will be of particular interest to those companies that have a requirement to report safety events to the PDMA in Japan in a timely and efficient manner that is integrated within their global safety reporting functions. This webinar will provide you with: -- An overview and the business benefits of Oracle Argus Safety Suite -- The business benefits of Oracle Argus Safety Japan and integrating it with Oracle Argus Safety -- The benefits of a single global safety database and why Oracle Argus Safety Suite is the right solution for it To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/7c7u5r7hi3qr. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 1255 BioPharmSystems
Argus Safety | Migrating Safety and Pharmacovigilance Data to Oracle's System
 
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Learn how to successfully approach a drug safety and pharmacovigilance system (e.g., Argus Safety) migration project. -- With the advancement of technology and the high cost of maintaining legacy safety and pharmacovigilance systems, organizations are forced to migrate to the latest technologies such as Argus Safety, that offer the most beneficial and relevant features. Compliance and business risks associated with safety data and the real potential for migration error (mapping errors, different dictionary maintenance practices, and MedDRA/WHO coding inconsistencies) introduces significant challenges, or an opportunity to excel. BioPharm Systems and Valiance Partners, together, offer a comprehensive solution that can tackle even the most complex migrations and implementations. With a cost-effective overall strategy that incorporates proven technology and business processes, your organization can ensure a successful migration and implementation while identifying and mitigating risk. Please join BioPharm Systems' Dr. Rodney Lemery and Valiance Partners' Richard Higger for a free one-hour webinar that will explore: - The types of risks and challenges associated with safety data system migrations - How to successfully approach a safety and pharmacovigilance system migration and implementation project - The benefits of pre-configured migration software and automated migration testing (100% testing) - Examples of past migration and implementation projects - Your own migration questions and challenges To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/86w2rj3v7t5n. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 8138 BioPharmSystems
Using Siebel Clinical (CTMS) for Your Job
 
01:03:31
Learn how Siebel Clinical can be used by the six most common clinical trial management job functions. -- Siebel Clinical is well-known as a robust clinical trial management system (CTMS) that streamlines clinical trial management. The system can be operated uniquely by users in various roles at sponsor and clinical research organizations. So in your current position, how would you use Siebel Clinical? Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this free one-hour webinar that explores how Siebel Clinical can be used by the following six most common clinical trial management job functions: -Clinical Administrator -Clinical Document Associate -Clinical Finance -Clinical Research Associate / Monitor -Executive -Study Manager To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/vk4l6d8pewzg. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 963 BioPharmSystems
Using Oracle's Empirica Topics for Signal Management
 
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Learn why and how Empirica Topics should be implemented and used to strengthen an organization's pharmacovigilance systems and processes. -- Signal management, the detection, prioritization, and evaluation of signals, is a crucial activity that life sciences organizations should continuously perform in an effort to ensure their products are not related to excessive risks in relationship to the products' benefits. With the emergence of comprehensive and user-friendly signal management solutions, the management of signals has become easier and more effective. Oracle's Empirica Topics is a powerful tool that helps companies track information and activities that are related to potential safety and pharmacovigilance signals. For example, after the creation of a signal topic, it can be delegated to members of a safety team for documenting the prioritization and evaluation of the signal. This transparent and collaborative process can protect your organization in an audit and ensure you have a well-established methodology for signal management. Join BioPharm Systems' Dr. Rodney Lemery, vice president of safety and pharmacovigilance, for this free one-hour webinar that will explore why and how Empirica Topics can be: 1. Implemented and configured using BioPharm's unique methodology 2. Utilized to strengthen your pharmacovigilance systems and processes, by employing techniques promoted by the Council for International Organizations of Medical Sciences (CIOMS) Working Group VIII To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/i3rrj625xa5j. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 2941 BioPharmSystems
Electronic Trip Reports in Siebel Clinical (CTMS)
 
01:01:19
Learn about the trip report functionality in BioPharm's pre-configured and enhanced version of Oracle's Siebel Clinical (CTMS) called ASCEND. -- Site visit and clinical trip reports are part of every clinical trial. In the past few decades, several tools have been developed to streamline the trip report process. And yet, organizations have shied away from using these tools to their full potential because they are uncertain how to interpret 21 CFR Part 11 as it pertains to electronic signatures. Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this one-hour presentation in which he will demonstrate how site visit SOPs can be translated into electronic trip report templates in Siebel Clinical, and then completed, reviewed, and approved -- entirely electronically. This webinar includes a live demonstration of the trip report functionality in BioPharm's pre-configured and enhanced version of Oracle's Siebel Clinical called ASCEND. To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/vaffumuveu0b. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 1624 BioPharmSystems
Open UI: The New Face of Siebel CTMS
 
01:00:36
Learn about Siebel Clinical (CTMS) Open UI. -- Oracle recently unveiled a new version of Siebel Clinical, a highly-sophisticated clinical trial management system (CTMS) used by life sciences companies, big and small. The latest major release, frequently referred to as Open UI or 8.1.1.11, provides users and administrators with more freedom and flexibility than ever before. Join us for a free one-hour webinar in which BioPharm's Param Singh, vice president of clinical trial management solutions, will review the new enhancements that have been introduced in the CTMS. After the presentation, attendees will have a better understanding of the: -- Features and benefits of Open UI -- Open UI implementation process -- Open UI upgrade considerations and process In addition to looking at the new capabilities, a brief demonstration of Open UI will be provided. To view this webinar in its entirety, please visit: https://cc.readytalk.com/r/dhrk6p49ih1e&eom Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/+BioPharm
Views: 519 BioPharmSystems
Future of Oracle Clinical, Oracle RDC, and Oracle TMS
 
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Learn about Oracle's continued commitment to the development and support of OC/RDC/TMS. -- It is no secret that most sponsors and clinical research organizations consider Oracle Clinical (OC), Remote Data Capture (RDC), and Thesaurus Management System (TMS), the most comprehensive clinical systems on the market. It is also no surprise that even with the arrival of numerous new systems since OC's inception in the mid-1990s, OC, RDC, and TMS have continued to thrive, due to their affordability, scalability, and improved system functionalities related to the complex clinical study design, performance, interface, and flexibility requirements of today's clinical trials. Whether your organization conducts electronic clinical trials or paper clinical trials, these systems simply provide the best return-on-investment. Please join BioPharm Systems' director of client relations, Vicky Green, and special guest from Oracle, director of product strategy, Chris Huang, for a free 60-minute webinar in which they will: -- Discuss the future of OC/RDC/TMS -- Share a sneak peek into the improved features in the current release of OC/RDC/TMS -- Highlight Oracle's continued commitment to the development and support of OC/RDC/TMS -- Host a live Q&A session with webinar participants To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/umijl2vtq2mm. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 1906 BioPharmSystems
Building an Effective Clinical Trial Management System (CTMS) Training Program
 
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Learn how to build an effective clinical trial management system (CTMS) training program. -- User adoption is the key to achieving a rapid ROI for your CTMS and the key to user adoption is an effective training program. Such training programs are based on a careful analysis of an organization's culture and the characteristics of its end-users. All training programs should be multi-faceted, comprehensive, and long-term in scope. But, depending on the organization, the details of a program should be tailored to meet the needs of the end-users and the organization as a whole. Effective CTMS training programs leave users feeling well-equipped to begin using the system and fully supported as they master it. Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this one-hour presentation on a variety of methods for achieving these goals and discussion on how to choose from these methods to build a training program that is right for your organization. This webinar will answer the following key questions: -How do adults learn? -What are the different approaches to software training? -Which approaches make sense in different types of organizations? -How can we best prepare users to start using the system? -How can we continue to support users over time? To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/u54aqy1svuto. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 2357 BioPharmSystems
How to Easily Copy, Migrate, and Archive Oracle Clinical Studies and Global Libraries
 
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Learn how to copy, migrate, and archive Oracle Clinical studies and global libraries, as well as refresh study patient data with Accel-Copy. -- Is your clinical systems production environment bloated with studies that should be archived? Do you long for an easy way to create and refresh a training environment? Are you struggling with the complexities of migrating studies to a new environment? Does your clinical team desire the power of diagnosing production issues in a test environment without having to involve a database administrator? Look no further. Accel-Copy can do all this and more! BioPharm Systems has developed Accel-Copy to be a versatile tool that allows your clinical environment to be managed by your clinical team more effectively. Out of the box, the application provides the following features and benefits: Database Management • Migrate select global library domains/studies • Archive studies/global library to an archival instance Support and Training Functionality • Refresh studies or parts of studies from production to development or QA • Refresh patient data/discrepancies from production to development or QA • Create/refresh training instance studies or parts of studies Clinical Administration and Configuration • Synchronize reference code lists among environments • Refresh sites and investigators among environments without replication • Manage organization units, regions, programs, and projects across environments from a single source Data Quality • Perform field by field comparisons of database data before and after a migration/upgrade • Copy global library domains from production to QA • Copy a new study to production from QA The application is fully documented, validated, and GxP compliant. To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/lgelz9jfs64u. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 1437 BioPharmSystems
Creating One Global Oracle Argus Safety System
 
58:26
Learn about a recent project for a top pharmaceutical company that entailed the merging of multiple drug safety systems. -- Many sponsors and CROs rely on an IT infrastructure that includes multiple disconnected safety and pharmacovigilance systems that vary by region and vendor. Although merging these systems into a single global solution may seem daunting and provide you with many technical challenges, it could be a crucial goal on the horizon for your organization. Please join BioPharm Systems' Dr. Rodney Lemery, vice president of safety and pharmacovigilance, for this free one-hour webinar in which he will review a recent project for a top pharmaceutical company that entailed the merging of multiple drug safety systems into one global Argus Safety pharmacovigilance system. Specific topics that will be examined include: -Adverse Event Case Migration -Merging and Configuring -Data Cleansing and Consistency -Configuring Reporting Rules To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/kuqj4f3gwl42. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 1979 BioPharmSystems
Oracle Clinical / Remote Data Capture (RDC) Implementation
 
01:00:59
Learn various Oracle Clinical and Remote Data Capture (RDC) implementation and usage best practices that sponsors and CRO's should consider to greatly increase the usability of the applications. -- As your organization implements or upgrades to a newer version of Oracle Clinical (OC) and Remote Data Capture (RDC), there are many considerations to take into account. Educating yourself on best practices and learning from past mistakes are all are critical components for a successful installation of your clinical data management and EDC systems, and the establishment of good standards. Join BioPharm Systems' Lori Venable, principal consultant, clinical data management, for this one-hour session that examines various OC and RDC implementation and usage best practices that all sponsors and CROs should consider to greatly increase the usability of the applications, as well as boost user productivity. This webinar covers best practices in the following areas: -Training -User roles and functions -SOPs and Work Instructions -Implementation, upgrade and usage standards -... and much more! To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/arw8mwj921fw. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 1385 BioPharmSystems
Oracle Clinical Development Analytics (CDA) Overview
 
01:27
Learn about Oracle Clinical Development Analytics (CDA). -- Oracle CDA is a clinical data analytics solution developed to work with various clinical and pharmacovigilance systems. Right out of the box, it works with Siebel Clinical, Oracle Clinical, and Remote Data Capture (RDC). CDA offers pre-built reports and dashboards that allow you to track progress and answer your clinical data management and clinical operations questions. If you are a sponsor or CRO seeking timely, fact-based insight into your clinical programs to bolster productivity and reduce costs, CDA is good solution to evaluate. For more information about CDA, visit http://www.biopharm.com/practices/clinical-data-warehousing-and-analytics/clinical-development-analytics.aspx.
Views: 238 BioPharmSystems
How St Jude Medical Manages Oracle Clinical Studies Using Accel-Copy
 
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Learn how St. Jude Medical streamlines the management of studies using an Oracle Clinical accelerator developed by BioPharm. -- St. Jude Medical, a Fortune 500 medical device company, leverages Accel-Copy to accelerate and streamline their processes related to Oracle Clinical studies. Since 2012, the company has been actively using BioPharm's Oracle Clinical accelerator for various activities, including: -- Testing new studies and study changes that are set up in a production environment, before releasing them -- Troubleshooting production issues -- Copying specific production studies for development efforts -- Training users on studies Please join St. Jude Medical's Ilya Gubernik, clinical software engineer, and BioPharm's Michelle Engler, director of application development, for a one-hour presentation that will discuss why and how St. Jude Medical uses Accel-Copy for its clinical studies. To view this webinar in its entirety, please visit: https://cc.readytalk.com/r/ot7mveyrd6kg&eom Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/+BioPharm
Views: 372 BioPharmSystems
Clinical Trial Supply Management with Siebel CTMS
 
57:31
Learn how Oracle's Siebel Clinical Trial Management System (CTMS) can be used for clinical trial supply and inventory management. -- Clinical supply and inventory management is a crucial part of the clinical trials process. Tracking investigational product and ancillary supply shipments to a site -- including quantities, lot numbers, and dates -- can help sponsors and clinical research organizations (CROs) save money and prevent headaches. Wouldn't it be nice if all the tracking could be done within a clinical trial management system (CTMS)? Well, we have good news: with Oracle's Siebel CTMS, it can. Clinical supplies can be tracked within Siebel Clinical right out-of-the-box. However, simple extensions, such as adding fields to an existing screen, and more complex enhancements, like adding new screens or an entire clinical supply management module, can make the tracking process more efficient, useful, and compliant. Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this complimentary 60-minute webinar in which he will: -- Discuss the struggles associated with clinical supply management and offer potential solutions -- Outline ways to use Siebel Clinical to track clinical supply inventory levels with and without system modifications -- Demonstrate how companies are currently tracking clinical supply and inventory with Siebel Clinical To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/nzfcucjgo4gn. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 1683 BioPharmSystems
Integrating Siebel Clinical with Argus Safety and a Legacy Product Issue System
 
02:54
Param Singh, Vice President of Clinical Trial Management Solutions, discusses integrating BioPharm Systems' pre-configured Siebel CTMS, BioPharm's ASCEND, with Argus Safety and a legacy product issue system. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 1464 BioPharmSystems
Leveraging Oracle's Life Sciences Data Hub (LSH)
 
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Learn how to dynamically select patient subpopulations with Oracle's Life Sciences Data Hub (LSH) and automatically deliver the longitudinal data for those subpopulations for detailed analysis. -- Oracle's Life Sciences Data Hub (LSH) is a framework that allows sponsors and clinical research organizations to manage clinical trial research data. One of the most difficult tasks in clinical research is the ability to rapidly bring together and analyze all the relevant data from multiple clinical trials for specific patient subpopulations. This information can be used for many business objectives including monitoring safety risks, planning future trials, and product defense. Join BioPharm Systems' Michael Grossman, vice president of clinical data warehousing and analytics, for a free one-hour session on an application within LSH that allows users to dynamically select patient subpopulations and automatically deliver the longitudinal data for those subpopulations for detailed analysis. You will learn how LSH can: -Provide dynamic selection of patient subpopulations and automatically generate a longitudinal data mart of the selected subpopulation -Save and reuse analysis methods and results for future analysis and exploration To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/mztuhxrl8hm6. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 1175 BioPharmSystems
How to Personalize Your Siebel Clinical (CTMS) User Interface
 
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Learn about the various ways one can personalize their Siebel Clinical Trial Management System (CTMS) user interface. -- You probably know that Oracle's Siebel Clinical application is the most configurable clinical trial management system (CTMS) on the market. But did you know that you, as an individual user, can modify Siebel Clinical in myriad ways to support your specific job? Features that can be personalized include: -Home Screen: Modify the layout to only include data types that are relevant to you -List Applets: Choose to display only the columns you need in the exact order you need them -- across the application -Queries: Create queries and save them to run at any time -User Preferences: Choose your printing settings, screen tab order, and even manage positions and passwords Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this complimentary one-hour session that will: -Explain many personalization features available in Siebel Clinical -Include a live demonstration of each feature discussed To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/g73leb4ioxoq. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 3047 BioPharmSystems
Implementing an Enterprise Clinical Trial Management System (CTMS)
 
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Learn about the various factors that sponsors and clinical research organizations (CROs) should consider when identifying the need for a comprehensive clinical trial management system (CTMS) and preparing for an implementation. -- How does a sponsor or clinical research organization (CRO) know when it is time for a comprehensive clinical trial management system (CTMS)? How does an organization prepare for the change and choose the right system? Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this free one-hour session in which he will: -- Shed light on the key indicators that point to the need for an enterprise CTMS -- Take a deep dive into the internal analysis necessary for identifying process changes and system requirements -- Explain how to get different stakeholders on board and excited -- Provide guidance on an effective vendor selection process To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/2g3456g19jil. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 251 BioPharmSystems
Siebel Clinical Best Practices: Post Implementation
 
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Learn about various best practices that sponsors and CRO's should consider once they have implemented a clinical trial management system (CTMS), such as Siebel Clinical. -- Has your organization recently implemented Oracle's Siebel Clinical as their CTMS? Or are you preparing to do so, or perhaps beginning to consider it? Regardless of your stage in the process, organizations that follow a set of best practices with Siebel Clinical enable users and administrators to operate efficiently and effectively. Best practices maximize the system's functionality, maintain consistent business processes, and ensure clean records. In short, they save you time and money. Join BioPharm Systems' Alice Crawford, senior consultant, clinical trial management solutions, for this one-hour session that will examine various best practices that life sciences organizations should consider once they have implemented a CTMS. This webinar covers best practices in the following areas: -SOPs -User responsibilities and positions -Record format conventions -Record entry and deletion -Template creation and use -Site visits and monitoring reports -Protocol amendments -Investigator payments -Change control tools -Querying and ad hoc reports -And much more! To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/hpv49yucxu9u. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc
Views: 261 BioPharmSystems
Strategies for Continuous Clinical Trial Management System (CTMS) Improvement
 
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Learn how sponsors and clinical research organizations (CROs) should plan a short-term and long-term roadmap that meets the expectations of a clinical trial management system's (CTMS) end-users. -- Whether you are an organization who had just implemented a clinical trial management system (CTMS) or an organization that has had a CTMS for a while, it is always a challenge to plan a short-term and long-term CTMS roadmap that meets the expectations of end-users. Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this free one-hour webinar that will address the following questions that a sponsor and clinical research organization (CRO) should consider when developing a CTMS continuous improvement plan: -- Who should be involved, as a stakeholder, in the development of a roadmap? -- How frequent should the change control board meet? -- What is the scope of the continuous improvement plan? -- Where should you gather input for the continuous improvement plan? -- What information should be captured for system enhancements? -- How should you prioritize future system enhancements? To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/82ib99cm3st. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 602 BioPharmSystems
Cloud-based vs. On-site Clinical Trial Management Systems (CTMS)
 
01:02:21
Learn the pros, cons, and risks that organizations should consider when deciding whether to host their clinical trial management system (CTMS) in the cloud. -- More and more sponsors and clinical research organizations (CROs) are moving their clinical applications to the cloud, seeking faster implementation timelines and reduced maintenance costs. Nonetheless, some organizations are hesitant to make the move because they are not sure how to navigate the risks and benefits of having a third party manage their servers and applications in remote data centers. In this free one-hour educational webinar, Param Singh, vice president of clinical trial management solutions, BioPharm Systems, will share the pros, cons, and risks that organizations should consider when deciding whether to host their clinical trial management system (CTMS) in the cloud. He will be joined by special guest, Sally Sweeney, director of validation, BioPharm Systems, to discuss the validation implications of hosting clinical systems. To view this webinar in its entirety, please visit: https://cc.readytalk.com/r/g8yqq3tcncvs. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 641 BioPharmSystems
Exploring Metrics in Siebel Clinical (CTMS)
 
01:07:06
Learn about the key metrics available in Siebel Clinical, Oracle's clinical trial management system (CTMS), and how to get them out of it. -- Siebel Clinical is a clinical trial management system (CTMS) known for its robust ability to track trial information, but we can still struggle from time to time when it comes to understanding what key metrics are available in the system, and how to get them out of it. Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this free one-hour webinar in which he will answer the following questions about Siebel CTMS and metrics: -- What categories of metrics are available in Siebel Clinical? -- What metrics are available within those categories? -- What additional metrics are available in Siebel Clinical via simple data manipulation, system configuration, and add-on tools and modules? -- How do you apply these metrics in clinical operations and trial management? To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/6mvwwwus7eic. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 341 BioPharmSystems
Create Accounts and Reset Passwords in Oracle Clinical, RDC, and TMS
 
54:09
Learn about Accel-Account Manager, an all-in-one solution for managing OC, RDC, and TMS accounts. -- With so many organizations using Oracle Clinical, Remote Data Capture (RDC), and Thesaurus Management System (TMS), it is no surprise BioPharm Systems' clinical account management solution, Accel-Account Manager, has generated a tremendous amount of interest and is now already in use at several organizations. Accel-Account Manager, a fully-documented, validated and GxP-compliant application, provides the ability for creating, updating, resetting, locking, unlocking, and mass creation of Oracle Clinical, RDC, and TMS user accounts. In addition, the application supports the management of database roles, OC study access, RDC study site privileges, and Oracle profiles. With Accel-Account Manager, end-users even have the ability to reset passwords, retrieve accounts, and manage security questions autonomously. An administrator can even create multiple accounts from an Excel spreadsheet and apply RDC security settings to several accounts with one simple click. Please join Michelle Engler, the creator of Accel-Account Manager, for this free one-hour presentation that will include a live demonstration of this all-in-one solution for managing your OC, RDC, and TMS accounts. To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/439uw4k1ogea. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 381 BioPharmSystems
Sharing Clinical Trial Management System (CTMS) Data Between Sponsors and CROs
 
01:00:48
Learn about the trend of outsourcing clinical trial management, as well as the various approaches to sharing clinical trial management system (CTMS) data between sponsors and CROs. -- There is a clear trend in the life sciences industry toward outsourcing clinical trial management to clinical research organizations (CROs). If your organization is considering outsourcing, or already does so, there are different methods that pharma and medical device companies can use to collect clinical trial management system (CTMS) data from their CRO partners. Join BioPharm Systems' Param Singh, vice president of clinical trial management solutions, for this free one-hour webinar in which he will discuss the overall outsourcing trend, as well as the pros and cons of the various approaches to sharing CTMS data between sponsors and CROs. To view this webinar in its entirety, please visit: http://www.biopharm.com or https://cc.readytalk.com/r/7zbwtinipyge. Twitter: http://www.twitter.com/BioPharmSystems Facebook: http://www.facebook.com/BioPharmSystems LinkedIn: http://www.linkedin.com/companies/biopharm-systems-inc Google+: https://plus.google.com/104105608638786200757
Views: 352 BioPharmSystems

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