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.