- Class II and III medical devices
- US/EU regulations (including FDA 21CFR Part 820, MDD, and ISO 13485)
- Quality system regulations
- Complaint handling
- Auditing
- Document control
- Business system analysis and change
We鈥檝e updated our privacy policy so that we are compliant with changing global privacy regulations and to provide you with insight into the limited ways in which we use your data.
You can read the details below. By accepting, you agree to the updated privacy policy.
