Process Validation for Manufacturing of Terbinaforce Tablets: Process Validation - Softcover

Kumar, Praveen; Chaudhary, Meenu

 
9786202553414: Process Validation for Manufacturing of Terbinaforce Tablets: Process Validation
Softcover
ISBN 10: 6202553413 ISBN 13: 9786202553414
Verlag: LAP LAMBERT Academic Publishing, 2020

Inhaltsangabe

SUMMARY- Validation is the way toward building up narrative proof exhibiting that a system, process, or movement did in testing and afterward creation keeps up the coveted level of consistence at all stages. In the pharmaceutical business, it is imperative that notwithstanding last testing and consistence of items, it is additionally guaranteed that the procedure will reliably deliver the normal outcomes. Validation mainly Based on, FDA regulations describing current good manufacturing practice (CGMP) for finished pharmaceuticals are provided in 21 CFR parts 210 and 211.A wide variety of procedures, processes, and activities need to be validated, the field of validation is divided into a number of subsections including the following:• Equipment validation• Facilities validation• HVAC system validation • Process Validation• Analytical method validation• Computer system validation• Packaging validation• Cold chain validation need of Process Validation for Assurance of quality of the product.

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Über die Autorin bzw. den Autor

Author's vita: Dr. Praveen Kumar, INSPIRE Faculty, CSIR-CSIO, Chandigarh, India. Ms. Pooja Devi, Scientist, CSIR-CSIO, Chandigarh, India. Dr. Mahesh Kumar, Scientist, CSIR-NPL, Delhi, India. Prof. S. M. Shivaprasad, ICMS, JNCASR, Bangalore, India.

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Verlag
LAP LAMBERT Academic Publishing
Erscheinungsdatum
2020
Sprache
Englisch
ISBN 10 
6202553413
ISBN 13 
9786202553414
Einband
Taschenbuch
Anzahl der Seiten
60
Kontakt zum Hersteller
Nicht verfügbar
Verantwortliche Person
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