Back to On-demand Webcast: How to Prepare for IDMP in Light of Continued Delays
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On-demand Webcast: How to Prepare for IDMP in Light of Continued Delays

An on-demand recording of the Veeva Sponsored Webcast, How to Prepare for IDMP in Light of Continued Delays originally recorded on 29 March 2017.


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Wednesday, 29 March 2017
12:00-1:30pm ET

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While IDMP is delayed again, there is a global trend in regulations that demand greater sharing of SPOR data, so companies cannot sit back and wait. To prepare for IDMP, ICSR E2B(R3), the Falsified Medicines Directive, and more, companies are...

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Fundamentals of US Regulatory Affairs, Eighth Edition

Table of Contents

Section I: General Information
Chapter 1 FDA and Related Regulatory Agencies
Chapter 2 History of Food, Drug and Cosmetic Law
Chapter 3 Overview of Drug, Biologic and Device Regulatory Pathways
Chapter 4 FDA Communications and Meetings
Chapter 5 Preparing for Key FDA Meetings and Advisory Committee Meetings
Chapter 6 Crisis Management
Chapter 7 Health Technology Assessment
Chapter 8 Good Laboratory Practice Regulations
Chapter 9 Clinical Trials: GCPs, Regulations and Compliance
Chapter 10 Current Good Manufacturing Practice and Quality System Design