Conference & Events
Documentation is the cornerstone of any company’s quality management system and is an essential GMP requirement. It is critical that anyone dealing with GMP documents and documentation systems understand the regulatory requirements and adopts best practice. As such this course provides a step by step explanation of what to do when managing GMP documentation and documentation systems.
Date: 03 May 2012 09:00 - 17:00
RSSL Pharma Training
The Science & Technology Centre
Organiser(s): RSSL Pharma Training
Contact for Event Information
Name : Mrs Rachel Horton
Reading Scientific Services Ltd
The Reading Science Centre
Booking form or other file(s):
This course is appropriate to a wide ranging audience, from QA and QC, through to production and clinical trials professionals.
By the end of the course you will:
• Understand the GMP rules and guidelines associated with the preparation, completion and archiving of documentation
• Appreciate the importance of maintaining a
comprehensive documentation system