Description: Addressing issues at the forefront of interest for the Clinical Trial Materials Professional (CTMP), this Second Edition highlights the most critical concepts related to the planning, manufacturing, packaging, labeling, distribution, reconciliation, and quality and regulatory control of clinical trial materials. It offers authoritative chapters by esteemed researchers and consultants in industry on the current and evolving state of clinical supplies operations. Tracking emerging trends and the development of new technologies, this Second Edition helps the CTMP operate effectively in the international sphere and reviews regulatory processes for drug approvals in the United States and Europe.
Review Quotes: "This practical guideoffer[s] authoritative evaluations of the scientific & legal issues involved in the successful completion of clinical trials for marketing approval by regulatory agencies." -Unlisted Drugs (for previous edition) "very comprehensive on the subject and give[s] a lot of "how-to" information. "very well written and very much geared towards the US market and Food and Drug Administration requirements." -European Journal of Parenteral Sciences (for previous edition) "describes both the science and the management of product development and furnishes effective approaches for preclinical drug discovery." -BOOKNews on the Internet (for previous edition)