Post Market Surveillance

Acceptance is not the end of your success, the next step is to maintain compliance with ISO 13485 and 21 CFR Part 820. You will need to participate in after-sales monitoring activities to further monitor the safety and effectiveness of the medical devices you sell.

HMC will help you:

● Medical device risk management

● System tuning and optimization

● Develop a PMS plan

We will rely on your market to offer the most suitable solution.