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OverviewFull Product DetailsAuthor: G. E. PagetPublisher: Kluwer Academic Publishers Group Imprint: Kluwer Academic Publishers Weight: 0.410kg ISBN: 9780852001844ISBN 10: 0852001843 Pages: 128 Publication Date: July 1977 Audience: Professional and scholarly , Professional & Vocational Format: Hardback Publisher's Status: Out of Print Availability: Out of stock ![]() Table of ContentsSection One The Regulatory Viewpoint.- 1 Maintaining the creative balance.- 2 A Swedish regulatory viewpoint.- 3 The seven deadly sins-a U.K. view.- Section Two The Industrial Viewpoint.- 4 Some possible effects of the introduction of quality control systems on the discovery and safety evaluation of drugs.- 5 Quality control in an industrial laboratory.- 6 Good Laboratory Practices (GLPs) and the Bioresearch Monitoring Program.- Section Three The Independent Expert.- 7 Quality and integrity assurance.- 8 The importance of experimental design.- Section Four The Research Contractor.- 9 Quality assurance in contract research organizations.- 10 Some problems in good laboratory practice for a contract research laboratory.ReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |