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CenterWatch Announces GCP Questions, FDA Answers, 2021 Edition | ||
By: PR Newswire Association LLC. - 13 May 2021 | Back to overview list |
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FALLS CHURCH, Va., May 13, 2021 /PRNewswire-PRWeb/ -- GCP Questions, FDA Answers, 2021 Edition What constitutes a "certified copy" of an electronic record? What are the penalties for not complying with ClinicalTrials.gov reporting procedures? How should ongoing training efforts be documented? These are a few of the questions clinical research professionals have asked the Office of Good Clinical Practice (OGCP). It can only help to learn from questions others have already asked. Through this compilation of more than 100 questions and responses, GCP Questions, FDA Answers provides answers to questions about the many guidelines from the FDA, including those related to adverse events, investigator responsibilities, electronic medical records and data privacy protection. Find advice on some of the most difficult and important topics that you will face, along with documents and resources that will bring clarity to your practices. This book will provide answers to the following:
Guidelines and regulations from the FDA are always evolving. But one can better understand the many changes that have occurred with this book. Learn from the many responses other professionals have received and ensure you are prepared to keep the trial on track. Get answers — and ensure trial success — with GCP Questions, FDA Answers, 2021 Edition. Book Details: Price: Easy Ways to Purchase: About CenterWatch: Media Contact Michelle Butler, CenterWatch, 703.538.7600, mbutler@wcgclinical.com
SOURCE CenterWatch |
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Copyright 2021 PR Newswire Association LLC. | Back to overview list |