FDA Audit, Quality Assurance Practices, Responsibilities and Expectations

Date : 20th May 2021 to 21st May 2021

Place : United States, San Jose

Website :https://www.complianceonline.com/fda-eu-audit-quality-assurance-qsr-seminar-training-80474SEM-prdsm?channel=allconferencealerts

Contact Person:Ashutos Swain

Description:

It is no surprise to anyone who reviews regulatory citations to notice the number of deficiencies cited that are associated with quality systems. Today, the basis for all FDA audits both within the US and internationally is based on the quality systems approach and the six systems that comprise it. Whether the audit is a full or partial audit, the quality system within a company will always be inspected and this seminar will help review what are the expectations and the common areas to be familiar with. As a basis for regulatory audits, the quality system, its procedures and their implementation are reviewed to help verify the level of effectiveness in assuring consistent control and quality of materials, components and final product.

FDA Audit, Quality Assurance Practices, Responsibilities and Expectations will be held in San Jose,United States on date 2021-05-21

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Deadline for abstracts/proposals : 10th May 2021

Keynote Speakers :

Check the event website for more details.