Guidelines for FDA 21 CFR Part 11-compliant monitoring and mapping
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Date: November 20th, 2024
Time: 4-5 PM CET, 3-4 PM GMT, 9-10 AM CST
What are the 21 CFR Part 11 requirements? And how do you turn them into simple, actionable steps you can implement in your procedures? Learn the steps you need to take for achieving 21 CFR Part 11 compliant records.
Key takeaways
- Which records fall under 21 CFR Part 11?
- What are the actual requirements of 21 CFR Part 11 (for your audit trails, security procedures, etc.)?
- How do you turn the requirements into concrete processes ensuring your operation lives up to the standard?
- How can technology help?
Adam Hartmann-Kruckow ,Co-founder & CCO at Eupry
Jakob Konradsen,Co-founder & Chief Quality Officer at Eupry
Do you feel fully confident navigating the FDA’s 21 CFR Part 11 for your monitoring, mapping, and similar compliance practices?
21 CFR part 11 is somewhat of a holy compliance grail for any regulated company working in or with the US (yes, if you have any affiliation, it probably applies to you as well). Not complying with the standard can lead to anything from smaller non-conformities and CAPAs to audit failures and reputational damage.
Join Eupry’s Chief Quality Officer Jakob Konradsen and co-founder and CCO Adam Hartmann-Kruckow as they go through everything you need to know to keep your temperature monitoring and mapping processes up to standard.
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