Emerging Non Clinical Biostatistics in Biopharmaceutical Development - and Manufacturin

Table des matières

BACKGROUND. Introduction. ANALYTICAL METHOD. Statistical Methods for Analytical Procedure Development, Validation and Transfer. Parallelism Testing of Bioassay. Validation of Assay Linearity. ROCESS DEVELOPMENT. Residual Host Cell DNA Risk Assessment. Statistical Evaluations of Viral Clearance. Pre-filtration Bio-burden Testing. Process Validation and Verification. MANUFACTURING. Specifications.

A propos de l'auteur

Harry Yang, Ph.D., is senior director and head of the Non-Clinical Biostatistics Group at MedImmune, the global biologics arm of AstraZeneca headquartered in Gaithersburg, Maryland.

Résumé

The premise of Quality by Design (QbD) is that the quality of the pharmaceutical product should be based upon a thorough understanding of both the product and the manufacturing process. This state-of-the-art book provides a single source of information on emerging statistical approaches to QbD and risk-based pharmaceutical development. A comprehensive resource, it combines in-depth explanations of advanced statistical methods with real-life case studies that illustrate practical applications of these methods in QbD implementation.

Détails du produit

• Auteurs: Harry Yang, Harry (Medimmune Yang, Yang Harry
• Edition: Taylor & Francis Ltd.
• Langues: Anglais
• Format d'édition: Livre Relié
• Sortie: 01.12.2016
• EAN: 9781498704151
• ISBN: 978-1-4987-0415-1
• Pages: 386
• Thèmes: Chapman & Hall/CRC Biostatistics Series; Chapman & Hall/CRC Biostatistics Series
• Catégories: Sciences naturelles, médecine, informatique, technique > Médecine > Général; Medical research, Epidemiology & medical statistics, MATHEMATICS / Probability & Statistics / General, MEDICAL / Pharmacology, MEDICAL / Biostatistics, Biology, life sciences, Pharmacology, Probability & statistics, Pharmaceutical technology, Probability and statistics, Epidemiology and Medical statistics, Industrial chemistry and chemical engineering