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Implementation of Risk Evaluation and Mitigation Strategy (REMS) - What do you need to do now?

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Category enterprise risk management, operational risk management, enterprise risk management framework, risk mitigation strategies, risk management program REMS, Risk Mitigation, FDA Update, Medication Guide, REMS implementation, REMS submission, REMS regulations, Risk Minimization Action Plan (RiskMAPS),Risk Evaluation and Mitigation Strategy (REMS), Risk Management, Mitigation, Adverse Effects, Safe Use, Labeling, Pharmacovigilance, FDA Amendments Act 2007

Deadline: December 04, 2017 | Date: December 05, 2017

Venue/Country: Online, U.S.A

Updated: 2017-11-14 21:20:40 (GMT+9)

Call For Papers - CFP

Attendees will receive knowledge on important and essential requirements related to Risk Management for potential pharmaceutical adverse effects. This webinar will provide basic understanding of requirements for REMS and steps to consider for implementation.

Objectives of the Presentation:

Risk Management and Risk Minimization Action Plans 2005

Consequences of FDAAA 2007

Understanding the impact

Assessing the potential need for a REMS

Responding to a requirement for a REMS

Voluntary submission of a REMS

Implementing a REMS

For Registration:

Note: Use Promo Code HYED6Z and get 10% off on registration (Valid till DECEMBER 31st 2017)

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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