Inspection of Process Validation (e-book)

Συγγραφείς: GMP
ISBN: 9783958071209
Εκδότης: GMP Publishing
Σελίδες: 90
Έτος Έκδοσης: 2018

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Do your validation processes meet their specified requirements? This bilingual guide offers an excellent up-to-date approach on process validation. It facilitates the planning and execution of all necessary steps to be compliant.

What should validation documentation contain?
How does one implement continued process verification?
What is the role of risk management?
What receives particular attention during an inspection?

In this GMP Series e-book you will be given specific answers to these and other frequently asked questions.

The validation of processes is a primary requirement in the pharmaceutical industry. This Aide-Mémoire of ZLG is a structured guide for the planning and execution of process validation. New concepts for modern process validation are introduced and known facts are summarised.

Due to its importance for the pharmaceutical industry, the directive document was translated into English by the Maas & Peither AG, GMP-Publishing. With this volume, you receive a bilingual comparison with excellent practical applicability, also in an international context.

Don't miss out on your copy of Inspection of Process Validation!

Target group:

Persons who are responsible for the validation of processes in the areas of quality management, quality assurance, quality control and production
Engineering
Persons who are responsible for process validation documents
Suppliers of the pharmaceutical and active ingredients manufacturing industry

Technical Requirements

This file is in PDF format!
Filesize: 2,27 MB

To view PDF files, we recommend using the Adobe Reader.

https://get.adobe.com/de/reader/

The e-book is password protected to prevent copying and modification of content.

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