Date :
Place : United States, San Jose
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.Deadline for abstracts/proposals : 6th December 2020
Organized By :Complianceonline
Keynote Speakers :
Check the event website for more details.