There's still time to register for DIA's Regulatory Submissions, Information, and Document Management Forum! The management of regulatory information has a profound impact on operational efficiency across the organization, data quality, and ultimately, the ability of an organization to meet the needs of patients.
Along with experts and peers, you'll gain insight into current required data standards for regulatory submissions as well as ongoing initiatives that can impact systems and business processes. You will identify ways to integrate and leverage data, documents, and knowledge to provide better insights for business decisions. No matter which of the four tracks you choose—Regulatory Information Management (RIM) Business, RIM Technology, Electronic Document Management (EDM), or Electronic Regulatory Submissions (ERS)—you'll leave prepared to meet challenges for your organization and play a key role in moving shared regulatory submission discourse forward in 2020!
Get the official conference eBook!
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Learn Before the Forum
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Register for a primer and preconference short course to get a leg up on the forum sessions and save $100!*
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Short Course 1: Data at the Heart of Life Science Professionals: Instant Informed Decision-Making | February 10 | 8:30AM-12:00PM
Learn how regulatory information management system data can be used as a tool to safeguard patients throughout the product development and marketing lifecycle, while establishing a seamless regulatory process of value-added steps with identified owners and document processes.
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Short Course 2: Preparing and Submitting Standardized Study Data to FDA, Presented by FDA, CDER | February 10 | 8:30AM-12:00PM
Have questions about FDA requirements for Standardized Study Data Submission? Want to identify any potential, rejectable errors before FDA submission? In this course, you'll analyze Study Data Technical Rejection Criteria validation logic and use tools that are available for preparing the Study Data submission.
*Preconference primer and short courses require registration and an additional fee.
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Digital technology has the potential to revolutionize clinical trials. Take an active role in driving the field forward at DIA's Digital Technology in Clinical Trials conference, co-sponsored with the Critical Path Institute's ePRO Consortium! With three tracks—Clinical Operations, Technology, and Data—this conference will cover applications of digital technologies in clinical trials to: improve patient experience, ensure that trial endpoints are clinically meaningful and represent improved patient outcomes, improve trial design, facilitate the conduct and operation of clinical trials, and facilitate the collection and use of quality data for clinical study and regulatory decision-making.
The Keynote Panel Discussion, Patient Perspectives in Digital Health: Advances in Remote Assessments for Parkinson's Disease, will feature an in-depth perspective from thought leaders as to how mobile technology can be used to streamline clinical trial procedures while incorporating patient perspectives in trial design and execution to ultimately improve outcomes for research.
Take advantage of Early Bird Rates through February 6!
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We hope to see you soon!
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DIA | 800 Enterprise Road, Suite 200 | Horsham, Pennsylvania 19044-3595
T. +1.215.442.6100 or toll-free at +1.888.257.6457 | E. Americas@DIAglobal.org
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