Sponsors
1
Speakers
1
Attendees
100
This webinar provides an essential overview of implementing and optimizing digital records processes for 21 CFR Part 11 compliance specifically for pharmaceutical Quality Control environments. It covers the shift from manual to digital QC data, assessing compliance with quality guidelines, navigating compliance challenges, ensuring audit readiness, and successful implementation for particle analysis data.
Sales Specialist
Beckman Coulter Life Sciences
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