ISBN: 9781574910988 - how to develop and manage qualification protocols for fda compliance (12 risultati)

Hardcover. Condizione: New. Brand new book, sourced directly from publisher. Dispatch time is 7-8 days from our warehouse. Book will be sent in robust, secure packaging to ensure it reaches you securely.

Condizione: As New. Unread book in perfect condition.

Condizione: New.

Condizione: New.

Condizione: As New. Unread book in perfect condition.

Condizione: New. pp. 375 1st Edition.

Condizione: New. pp. 375.

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.

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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.…

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Condizione: New. pp. 375 This item is printed on demand.