When: |
16 Dec through 16 Dec 2020 | |
Where: |
Online Event | | |
Website URL: |
https://www.complianceonline.com/21-cfr-part-11-qms-software-risk-based-implementation-webinar-training-706363-prdw?channel=brownwalker | |
Sponsoring organization: |
Compliance Online | |
Categories: |
Business - Other |
Keywords:
Event 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.
Posting date:
09 August 2020 | 186 views
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