Clinical Research Compliance Manual: An Administrative Guide

For anyone receiving or applying for clinical research funding, Clinical Research Compliance Manual: An Administrative Guide covers today’s most crucial topics, including:

Human subject protections Institutional Review Board regulations and requirements Conflicts of interest Scientific misconduct Reimbursement issues And much more!

Clinical Research Compliance Manual helps you establish best practices and carry out all administrative tasks in a compliant manner while keeping you completely up-to-date on the most recent developments:

Covers the major clinical research issues - with chapters written by experts in the field Provides legal explanations of the major regulatory issues in an easy-to-understand format Includes summaries of federal regulatory agencies, analysis of major cases, flowcharts, checklists, and footnotes to compliance program development, auditing and monitoring

Clinical Research Compliance Manual has been updated to include:

Discussion on the revised Common Rule Analysis of enforcement of the May 25, 2018 GDPR New information on HHS’s updated informed consent in human subject research regulations commonly referred to as the 2018 Rules
Updated sections on NIH Supported Clinical Research, including a discussion of recent changes made to the Bayh-Dole Act of 1980 Revised sections on the categorization of medical devices as it pertains to reimbursement

And much more!