Phil geneva pharmaceuticals cloud (3 risultati)
Cloud, P: How to Develop and Manage Qualification Protocols
Phil Cloud (Geneva Pharmaceuticals Inc., Broomfield, Colorado, USA)
- Rilegato
Da: moluna, Greven, Germaniamoluna
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 70,67
EUR 48,99 spedizioneSpedito da Germania a U.S.A.Quantità: Più di 20 disponibili
Gebunden. Condizione: New. Phil CloudAll current Good Manufacturing Practices (cGMP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP) and ISO 9000 standards and regulations require that validation document be established and followed. Yet these regulations do no.
- Rilegato
Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 89,35
EUR 66,95 spedizioneSpedito da Germania a U.S.A.Quantità: 2 disponibili
Buch. Condizione: Neu. Neuware - Focusing specifically on the FDA documentation requirements, How to Develop and Manage Qualification Protocols for FDA Compliance provides readers with concrete guidance on how to develop and manage qualification protocols and their associated documentation to ensure that their companies are not…at risk. It discusses key function areas, such as cleaning, facilities and utilities, equipment, computers and software, and process in detail. The book contains 35 validation procedures and 30 forms that can be used to establish a validation documentation system and provides protocol templates readers can use as their own. Numerous diagrams and graphics are used to illustrate key points.
Cloud, P: Pharmaceutical Equipment Validation
Phil Cloud (Geneva Pharmaceuticals Inc., Broomfield, Colorado, USA)
- Rilegato
Da: moluna, Greven, Germaniamoluna
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 311,39
EUR 48,99 spedizioneSpedito da Germania a U.S.A.Quantità: Più di 20 disponibili
Condizione: New. Phil CloudWhile FDA regulations, cGMP, GLP, GCP, and the industry standard ISO 9000 require that documentation be established and followed, they do not provide guidelines on how to produce that documentation. Pharmaceutical Equipment Validation gives de.
