Need Assistance with any or all of the Following

Design Development and/or Documentation of your medical Device ?

Click Submit for Free Evaluation and Receive a Timeline, Budgetary Estimate and Regulatory Go To Market Strategy

21 CFR part 820 IEC62304 ISO14971 And More
21 CFR Part 11 ISO13485 IEC60601
ISO10993 IEC62366 ISO14155
European Medical Device Regulation (MDR)