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.
General
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