CFR-11
CFR
Hi,
Thank you for taking the time to leave your request. Good news! We will be working on FDA CFR Part 11 compliance soon. It will be available in one of our upcoming releases. We will be communicating it through our product newsletter, via an alert inside PandaDoc, and here in our Idea Portal, so stay tuned!
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Kevin Funk commented
I have a prospect who works in Clinical Research and looking for an e-signature platform that offers 21CFR Part 11 compliance before she decides to move forward with exploring PandaDoc as a potential solution. I've also had this come up many times before- huge deal breaker.
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Ekaterina Kuchuk commented
Was asked by a current client, might impact their decision to renew
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Zachariah Lovelace commented
I had a customer ask if we are 21CFR11 compliant. The bio-pharm industry is one that we can go after
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mchelala commented
Critical requirement by the FDA for all medical devices and pharmaceutical companies
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Jean-Yves Pairet commented
Required in the medical device industry for esignature software tools.
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Chad Nuss commented
We need to solve this ASAP.
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Scott Klepfer commented
21 CFR Part 11 Compliance on e-sigs is crucial in the pharma industry for quality docs. Highly recommend adding this feature.
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Thomas Kiesnowski commented
This item is a real deal breaker.
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Tiffany Quillan commented
Critical for us - thank you!
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AdminJamie Venice (Admin, PandaDoc) commented
This has come up multiple times on phone calls which is a big deal breaker for potential customers
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Ben Richardson commented
21 CFR Part 11 Compliance is the biggest deal break our team deals with on a daily basis and this metric is not tracked as well as it should be.
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Lonnie Oxendine commented
SUPER IMPORTANT
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Tanner Deans commented
Was asked about this today from a prospect.