Understanding 21 CFR 11 and Data Integrity Regulations [Webinar Deck]
Complying with the new, more demanding requirements and bringing manufacturing processes and control to a new level is a challenge that cannot neglect full data integrity related standards compliance.
Download this webinar to learn:
- How to minimize the risk of non-conformances by understanding your processes
- The importance of cultivating an ethical approach to data management
- How to become and stay compliant, and prepare for future standard changes
Complete the form to download the webinar
Looking for a 21CFR Part 11 Solution for your cleanroom data. Look no further than PharmaIntegrity.
PharmaIntegrity Data Management System for Pharmaceutical Industry Data Integrity (21CFR11)
Relevant 21CFR Part 11 Data Integrity Materials
https://www.pmeasuring.com/blog/data-trending-annex-1-alert-levels/
https://www.pmeasuring.com/blog/new-normal-data-integrity-esignatures/
https://www.pmeasuring.com/blog/remote-audits-new-normal-21cfr11/
https://www.pmeasuring.com/blog/new-normal-particle-counter-data-remote-access-electronic-signatures/
https://www.pmeasuring.com/blog/electronic-data-in-pharmaceutical-manufacturing-microbial-monitoring/
https://www.pmeasuring.com/blog/data-integrity/
21 CFR Part 11 and Data Integrity Regulations Frequently Asked Questions
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