Conferences
Conference Details
Laboratory Inspection and Auditing
Date :
Place : United States, San Jose
Contact Person:Ashutos Swain
Description:
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 Understand the key steps in the analytical process Recognize commonly-used analytical techniques and instruments Appreciate the significance of pharmacopoeias in analytical operations Understand the requirements for controlling reference standards, reagents and important consumables Appreciate the importance of GMP controls over analytical method suitability (validation, verification and transfer) Classify analytical instruments according to quality risk and understand the qualification requirements for each class Understand current expectations for data integrity controls, including electronic data systems Identify non-conformances in the control of stability studies Appreciate the regulatory requirements for reference and retention samplesLaboratory Inspection and Auditing will be held in San Jose,United States on date 2021-09-23
Deadline for abstracts/proposals : 13th September 2021
Organized By :Complianceonline
Keynote Speakers :
Check the event website for more details.
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