Does implementing electronic records and signatures in your software meet 21 CFR Part 11 requirements? Does your software properly take care of data integrity and traceability?

If you plan to sell your software to companies that need to meet regulatory requirements in pharma, biotech, medical device, and other industries, then 21 CFR part 11 features should be an essential part of your software.

Watch the webinar and discover:

    ✔  Expert advice on practical implementation

    ✔  Examples from the industry

    ✔  Answered questions from the audience

Read more about our expertise. We are specialized in custom software development for life sciences, IVD and medical devices.

If you want to discuss the topic more in detail, get in touch with our experts and schedule a free 30-min consultation.