In FDA (U.S. Food and Drug Administration) and ISO 27002 compliant processes, digital signatures play a crucial role in ensuring the integrity, authenticity, and security of electronic records and signatures. The use of digital signatures is outlined in the FDA’s regulations, particularly in the context of electronic records and electronic signatures, as specified in Title 21 of the Code of Federal Regulations (CFR) Part 11 and ISO/IEC 27002:2013 respectively.
Digital signatures are not just for PDF documents though. Most FDA/ISO compliant processes require digital signature approvals for changes to software as well, also known as Pull Requests. Essentially files containing code are documents that need to undergo a strict review and approval process, just like any other controlled documents that are part of the change management.
Here are the key elements related to digital signatures, signing intent, and the role of the signee in an FDA/ISO compliant process:
Workzone for Bitbucket allows to configure signature reviewer groups
When reviewers approve a pull request they are asked to sign their approval with a personal token and select a role/intent.
All signatures, git commit hash and role/intent are safely recorded in the pull request’s history.
Visit Workzone for Bitbucket today!
As always,
Happy coding.
Sean
Sean Manwarring _Izymes_
Head of Marketing at Izymes
Izymes
Australia
2 accepted answers
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