Regulatory Post Market Surveillance Process
It's called medical device post-market surveillance (PMS), a system that provides continuous feedback about a device on the market in order to maintain a high standard of product quality. PMS is a regulatory requirement in major markets like Europe and the United States. The purpose of compliance is to ensure that the provisions of medical devices legislation are complied with after devices are placed on the market or put into service. It aims to ensure that non-compliant devices are removed from the market. Medical device manufacturers, as well as other firms involved in the distribution of devices, must follow certain requirements and regulations once devices are on the market

E & E Medicals will help you maintain Post market compliance in the following ways:
E & E Medicals and consulting Post Market Surveillance Experts shall help in coordinating and investigating customer complaints, makes an initial reporting decision, and ensures completeness and consistency of complaint and related documentation. Medical Device Post-marketing Vigilance Reporting. Assist you in Post-marketing Surveillance on your medical device while in the market.

To learn more about our postmarket Surveillance Compliance , contact us today