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OverviewFull Product DetailsAuthor: Sarfaraz K. NiaziPublisher: Taylor & Francis Ltd Imprint: CRC Press Edition: 2nd edition Weight: 1.192kg ISBN: 9781032931296ISBN 10: 1032931299 Pages: 646 Publication Date: 14 October 2024 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 ContentsBioequivalence Testing Rationale and Principles. Bioequivalence Testing Protocols-FDA-Compressed Dosage Forms. GMP Audit Template, EU Guidelines. Guidance on Formulating Compressed Solids. Appendix I: Dissolution Testing Requirements of Compressed Dosage Forms. Appendix II: Approved Excipients in Compressed Solid Dosage Forms.ReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |