by LorriA.Nesbitt (Author)
Nesbitt (PharmD) offers insight into the clinical research industry, the ethical principles of clinical research, the role of the institutional review board, evaluating the clinical trial protocol, the data management process, preparing for an FDA audit, working with research participants, negotiati
Format: Paperback
Pages: 274
Publisher: Jones and Bartlett Publishers, Inc
Published: 20 Jun 2003
ISBN 10: 0763731366
ISBN 13: 9780763731366