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This webinar discusses the FDA's expectations for enhanced data integrity in electronic records and signatures, covering crucial aspects of CGMP documentation and compliance in regulated sectors. It highlights concerns about system vulnerabilities, updates, and cloud-based software affecting data integrity, underlining the significance of accuracy and consistency in the data life cycle.
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Timings09:00 AM-06:00 PM (expected)Not Verified | Entry FeesCheck Official Website |
Estimated Turnoutupto 100 Delegates Based on previous editions | Event TypeWorkshop |
EditionsApr 2025+2 more editions Frequency Triennial Next edition likely in Apr 2028 | Official LinksWebsiteContacts Report Error Claim this event |
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ComplianceIQ USA1559 Total Events • 545 Followers | |
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Neha Kirni
Dhaval Gupta
Director
Minh Hoang
Nikhil Goenka
Murali Bharadwaz
Archit Jain
Kiran B.R.
Founder
Sanakkayala
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https://10times.com/hub/technology-hub
May 192025
Apr 302025