Conference & Events
The course addresses environmental monitoring for the manufacturing of both sterile and non-sterile products. It looks at the legislation and guidance available, techniques employed to monitor pharmaceutical environments, data trending and how to manage out of limit results. Additionally a review of risks associated with contamination sources, monitoring methods, trending and reporting of results is undertaken.
Date: 12 December 2012 09:00 - 17:00
RSSL Pharma Training
The Science & Technology Centre
Organiser(s): Reading Scientific Services Ltd
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