Conference Details

21 CFR Part 11 and QMS Software Risk-Based Implementation

Date :

Place : United States, San Jose

Website :

Contact Person:Ashutos Swain

Description:

CGMP-compliant companies must develop / implement formal software controls and usage, starting with proper verification and validation methods. This is an important consideration for a company’s Quality Management System (QMS) and must consider applicable elements of electronic records / signatures / Part 11. The US FDA recently added data integrity and cybersecurity to these requirements. These activities must be properly documented.

21 CFR Part 11 and QMS Software Risk-Based Implementation will be held in San Jose,United States on date 2020-12-16

Deadline for abstracts/proposals : 6th December 2020

Organized By :Complianceonline

Keynote Speakers :

Check the for more details.

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