Regulatory & Quality Services for Clinical, Manufacturing, & Laboratory Practices.
WHY GxP SUPPORT
Meeting the Challenge of Quality
GxP Support, Start to Finish
Follow Best Practices for:
- cGCP - Good Clinical Practice
- cGLP - Good Laboratory Practice
- cGMP - Good Manufacturing Practice
- 21 CFR § 11 requirements (electronic records, audit trails)
- 21 CFR § 820 requirements (quality for medical devices)
- European Economic Area CE marking
- Health-industry standards in other world regions, including the UK and EU
GxP SUPPORT DELIVERS
Industry-Leading Security, Quality, & Compliance
ENABLING YOUR SUCCESS
DNAnexus GxP Support experts are ready to help bring your drug or device development work into compliance, with all applicable best practice guidelines.