This text is an excerpt from the GMP Series Download Inspection of Process Validation
In this GMP Series Download you will be given specific answers to these and other frequently asked questions.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?
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.
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