Post-market surveillance has become an inexorable trend around the globe.

Therefore, proactively collect and track the following information of your products is essential and crucial.

-Relative post-market incidents reported (e.g. alerts, AEs, recalls)

-Relevant clinical literatures

 

By analyzing these data, you could

-Comply with international standards (e.g. MDD/MDR/ISO 13485) or regulations (e.g. GDP) of your countries.

-Detect potential risks and improve the quality and safety of your products.

-Further update your clinical evaluations, risk analysis and post-market follow-up.

 

We are especially specialized in the field and have access to multiple databases  in different languages/countries at your service.

Please check out the attached flyer for more details.