This is a great suggestion and we have had other customers asking about this feature as well. We are looking into the possibility of developing it, but it isn’t on our product roadmap for the next few months. Please feel free to upvote or leave your comment to let us know how and why this functionality is important for you.
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.
Ekaterina Kuchuk commented
Was asked by a current client, might impact their decision to renew
Zachariah Lovelace commented
I had a customer ask if we are 21CFR11 compliant. The bio-pharm industry is one that we can go after
Critical requirement by the FDA for all medical devices and pharmaceutical companies
Jean-Yves Pairet commented
Required in the medical device industry for esignature software tools.
Chad Nuss commented
We need to solve this ASAP.
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.
Thomas Kiesnowski commented
This item is a real deal breaker.
Tiffany Quillan commented
Critical for us - thank you!
Jamie Venice commented
This has come up multiple times on phone calls which is a big deal breaker for potential customers
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.
Lonnie Oxendine commented
Tanner Deans commented
Was asked about this today from a prospect.