Enter the first customer review for this item
This pdf download shows how you can establish an effective CAPA system, which interfaces there are to other systems and what content a CAPA SOP should have.
e-book / PDF-Download
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 pdf download 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:
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.
If you choose payment by bank transfer:
If you choose payment by credit card:
In this pdf download you'll find answers on how deviations are defined, what must be observed...
How can occured failures be avoided in the future? Start to treat the root cause, not the...
With this GMP newsletter you will be regularly informed on the latest developments in GMP.