21 CFR Part 11/Annex 11compliance is required by any medical device companies that wish to sell their devices in the US and EU.
21 CFR Part 11 is the part of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES). Part 11, as it is commonly called, defines the criteria under which electronic records and electronic signatures are considered trustworthy, reliable, and equivalent to paper records (Title 21 CFR Part 11 Section 11.1 (a)).
There is the “Paper” way, and there is the “Electronic” way. In order to comply with the 21 CFR Part 11, the software system must comply with a list of requirements. Orcnaos stands for all of these requirements and allows medical device manufacturers to use it’s software freely and dispose of any paper-based system they have.
Ensure compliance with 21 CFR Part 11 regulations and streamline your medical device development process with Orcanos. Our intuitive solution empowers you to meet the necessary requirements for selling devices in the US and EU. Simplify compliance with features designed to meet FDA guidelines, including electronic signatures, audit trails, and user authentication. Discover how Orcanos can help your organization achieve 21 CFR Part 11 compliance today.
You can easily sign all your electronic records and documents with Orcanos' Electronic Signature.
At Orcanos, logical accounts are restricted to authorized personnel who have been granted system access. This is managed through role-based permissions, which are assigned by user groups.
Take your regulatory compliance to the next level with Orcanos. Book a demo today and experience the power of our integrated solutions firsthand!
Orcanos allows producing visual displays of audit trails of electronic record data and their associated metadata to XML, HTML, Excel, MSWord.
Orcanos Cloud guarantees a reliable and secure backup service for all electronic data and documents.