ServiceUpdated on 28 October 2024
21 CFR Part 11 consulting
About
Our experts have hands-on experience in IVD medical device industry, clinical trials, and GxP-ready software development.
We assist you in conducting a gap analysis of your existing computer systems and software applications to identify areas of non-compliance. We then recommend best practices and technical solutions to ensure full compliance with the regulation.
Type
- Consulting
- Development
Applies to
- Life Science & Health Care
Organisation
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