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OverviewThis text lists the necessary steps for meeting compliance requirements during the drug development process. It presents comprehensive approaches for validating analytical methods for pharmaceutical applications. Full Product DetailsAuthor: Carmen MedinaPublisher: Taylor & Francis Ltd Imprint: CRC Press Weight: 0.911kg ISBN: 9780367394769ISBN 10: 0367394766 Pages: 704 Publication Date: 02 October 2019 Audience: Professional and scholarly , Professional & Vocational Format: Paperback Publisher's Status: Active Availability: In Print ![]() This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us. Table of ContentsReviewsThe book captures the reader's attention from the first chapter and paves a lively way for prosecution of further independent studies.One of those invaluable books which any reader will want to have beside him as he comes into face with questions of FDA's changing and regulatory demands. the strategies and programs offered in this book can significantly decrease a company's compliance vulnerability and regulatory liability and increase its overall quality. -Current Engineering Practice gives manufacturers sound, practical advise on inspection readiness and overall compliance. -E-Streams Author InformationCarmen Medina Tab Content 6Author Website:Countries AvailableAll regions |