A study of biopharmaceutical process validation. It aims to enable developers and producers to ensure safe products, reduce the risk of adverse reactions in patients, and avoid recalls by outlining sophisticated validation approaches to characterize processes, process intermediates, and final product fully. The text emphasizes cost effectiveness while determining what level of validation is required for different phases of development, license application, and process improvements.
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Regulatory trends related to process validation; a biotech validation concept; establishing process robustness using designed experiments; identification and establishment of operating ranges of critical process variables; cell line characterization; process validation and characterization; recovery operations; purification issues; validation of the purification process for virus clearance evaluation; chromatography media lifetime; validation of filtration; cleaning -multiuse facility issues; role of analytical testing in biopharmaceutical analysis; process validation in biopharmaceutical manufacturing; regulatory reform for biotechnology-derived products - the regulatory impact of process changes on validation; special issues for synthetic antisense oligonucleotides; special issues for DNA vaccines; process development and process validation for plasmid DNA vaccines; ex vivo autologous cell therapies.
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EUR 79,02 per la spedizione da U.S.A. a Italia
Destinazione, tempi e costiDa: Goodwill of Silicon Valley, SAN JOSE, CA, U.S.A.
Condizione: acceptable. Supports Goodwill of Silicon Valley job training programs. The cover and pages are in Acceptable condition! Any other included accessories are also in Acceptable condition showing use. Use can include some highlighting and writing, page and cover creases as well as other types visible wear such as cover tears discoloration, staining, marks, scuffs, etc. All pages intact. Codice articolo GWSVV.0824702492.A
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