# Using a risk-based approach to comply with 21 CFR Part 11

60

minutes

This browser does not support HTML video.

Click for sound

### Webinar Resources for complying with CFR Part 11

- [CSA: What FDA's new draft guidance means for the future of regulated software companies](/content/blog/computer-software-assurance?utm_source=webinar&utm_medium=slides&utm_campaign=part-11&utm_term=tof/index.html)
- [Why custom validating your development tooling is an anti-pattern](/content/blog/the-turtle-problem?utm_source=webinar&utm_medium=slides&utm_campaign=part-11&utm_term=tof/index.html)
- [Clinical Trial Computerized Systems Regulation Review](/content/blog/clinical-trial-computerized-systems-regulation-review?utm_source=webinar&utm_medium=slides&utm_campaign=part-11&utm_term=tof/index.html)