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4.00 RAC

Understanding & Managing the US Clinical Trial Process

This course provides an overview of the foundation for clinical trials in the US, including the types and phases of clinical trials and protocol development, as well as key issues related to clinical trial management and monitoring, are reviewed from a regulatory perspective.

4.00 RAC

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Clinical trials are an essential part of the evaluation of safety and efficacy for new drugs, biologics and medical devices, and are critical to obtaining regulatory approval as the final milestone in product development. As a regulatory professional, you have a significant role in clinical trial...

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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