Software Validation Process for 21 CFR Part 11 is all about authenticity and integrity of electronic signatures and records. Care should be taken to avoid confusion and get validation right.
The FDA’s Code of Federal Regulations (CFR) is a collection of laws that regulate the various government agencies. Different titles of the CFR govern respective regulated areas.
What is 21 CFR Part 11?
Codes contained in21 CFR Part 11 relate to electronic records and approval signatures, which are digital versions of paper documents and handwritten signatures. 21 CFR Part 11enables
- A paper record to be replaced by an electronic record
- Any handwritten signature to be replaced with an electronic signature
- The software of these systems to be validated, so that the authenticity of electronic signatures can be proven
- An organization to implement good business practices.
Why is software validation process for 21 CFR Part 11 necessary?
With the widespread proliferation, reach and prevalence of the use of computers; it is a given that people would like to use electronic records instead of paper records. CFRs became necessary as records graduated to the electronic format, because of which validation of these signatures for their authenticity also became necessary.
An intrinsic part of SOPs
The software validation process for 21 CFR Part 11 is enshrined in the regulated company’sStandard Operating Procedures (SOP’s), which describe the way in which processes are to be performed. In the course of implementation of the software validation process for 21 CFR Part 11; any paper record, inclusive of signatures, is to be replaced with an electronic one, given that the computer system is validated and has appropriate features.
Primary areas software validation process for 21 CFR Part 11 compliance
21 CFR Part 11 compliance consists of three primary areas:
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