Seminar - One Day Virtual Seminar Laboratory Inspection and Auditing When: Thursday Sep 23 - September 23 , 2021 DAY 01(10:00 AM - 5:00 PM)
Quality auditing of pharmaceutical quality control laboratories is an important activity for those performing due diligence or monitoring the performance of a sub-contractor. Besides covering GMP regulations affecting pharmaceutical quality control, this one-day course is designed to provide the non-specialist with the necessary knowledge to understand the quality significance and risk associated with different analytical operations.
By the end of the course, attendees will be able to:
Identify non-conformance to cGMP regulations in analytical operations
Recognize commonly-used analytical techniques and instruments
Understand the key steps in the analytical process
Understand the requirements for controlling reference standards, reagents and important consumables
Classify analytical instruments according to the quality risk and understand the qualification requirements for each class
Identify non-conformances in the control of stability studies
US and EU GMPs relating to quality control operations
Information provided by different analytical techniques
What are critical consumables and how should they be controlled?
Control of analytical methods over their lifecycle
Register soon because space is limited.
We hope you’re able to join us!