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The Clinical Audit in Pharmaceutical Development
0 - Default Title
Description
describes Good Clinical Practices (GCPs) and the role of regulatory agencies in the review, validation, and auditing processes
outlines the clinical process, from trial design through report writing
compares and contrasts United States and international regulatory statutes
identifies monitoring as the key to guaranteeing high-quality data
focuses on the role of the clinical audit in achieving unity in a multinational study
discusses the worldwide influence of the US Food and Drug Administration audit
analyzes findings from previous FDA clinical audits to reveal trends and future directions
provides guidelines for fraud detection and considers the ramifications of falsified data
and more!Confirming that all clinical information has been properly collected and reported, The Clinical Audit in Pharmaceutical Development is a crucial reference for clinical and research pharmacists and pharmacologists; biostatisticians; clinical research associates, coordinators, and investigators; quality control, quality assurance, and regulatory compliance managers; and upper-level undergraduate and graduate students in these disciplines.
Product details
Binding:
Paperback
Edition:
1
Number of Pages:
218
Release Date:
2019-09-27
Publication Date:
2019-09-05
Publisher:
CRC Press
Languages:
Original:
English
ISBN10:
0367399334
ISBN13:
9780367399337
Weight:
339 g
Height:
156 cm
Width:
234 cm
Thickness:
12 cm
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