Clinical Trials

Author: Tom Brody PhD University of California at Berkeley
Edition: 1
Binding: Hardcover
ISBN: 0123919118

Clinical Trials: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines

Clinical Trials: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines is a practical guidebook for those engaged in clinical trial design. This book details the organizations and content of clinical trials, including trial design, safety, endpoints, subgroups, HRQoL, consent forms and package inserts. It provides extensive information on both US and international regulatory guidelines and features concrete examples of study design from the medical literature. This book is intended to orient those new to clinical trial design and provide them with a better understanding of how to conduct clinical trials. It will also act as a guide for the more experienced by detailing endpoint selection and illustrating how to Categories: Clinical trials, Registries. Contributors: Committee on Clinical Trial Registries - Author. Format: Paperback Read medical textbooks online like Clinical Trials here

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Clinical Research Informatics

The purpose of the book is to provide an overview of clinical research (types), activities, and areas where informatics and IT could fit into various activities and business practices. This book will introduce and apply informatics concepts only as they have particular relevance to clinical research settings.

Categories: Clinical trials, Registries, Clinical trial. Contributors: Committee on Clinical Trial Registries - Author. Format: Paperback

Categories: Clinical trials. Contributors: Committee on Strategies for Small-Number-Participant Clinical Research Trials - Author. Format: Paperback

Clinical Trials Online

It will also act as a guide for the more experienced by detailing endpoint selection and illustrating how to

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