Understanding 21 CFR 11 and Data Integrity Regulations
Today, both the MHRA and FDA are highly focused on data integrity and currently discourage methods by which data is recorded manually. Modern data management systems provide a missing link in such circumstances, allowing secure data transfer, automated reporting without data integrity fears, and electronics batch release approval processes.
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.
Watch 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