The world’s most extensive GMP knowledge portal.
Enter the first customer review for this item
This e-book shows how you can establish an effective CAPA system, which interfaces there are to other systems and what content a CAPA SOP should have.
1st edition 2015
Delivery immediately after receipt of payment
Excerpt from the GMP Compliance Adviser Inadequate CAPA procedures continue to be among the leading findings in U.S. FDA and European GMP inspections. During the implementation of a CAPA system it should be ensured that the CAPA system is understood as an important element of the pharmaceutical quality system and, consequently, that it is implemented uniformly company-wide or group-wide, as a governing system. How to Manage Corrective and Preventive Actions (CAPA) in a GMP Environment is the ultimate guide on building and implementing an effective CAPA compliance program. The e-book shows how you can establish an effective CAPA system, which interfaces there are to other systems and what content a CAPA SOP should have. Here’s an overview of what you’ll discover in its pages:
Reading Sample "How to Manage Corrective and Preventive Actions (CAPA) in GMP Environment"
Please enter these characters in the following text field.
This file is in PDF format!Filesize: 864 KB
To view PDF files, we recommend using the Adobe Reader.
The e-book is password protected to prevent copying and modification of content.
Please note the following procedure guidelines:
For payment by invoice:
When paying by credit card:
The Newsletter of GMP-Verlag
News and upcoming trends: Stay up-to-date on the latest developments in GMP!
Please select your currency