If you work in the field of medical devices we encourage you to attend the MDR Conference on September 25 in Warsaw. Katarzyna Dulna – our Chief Medical Officer, will deliver presentation about the clinical trials for medical devices according to MDR 2017/745. You will gain the overview of the regulatory process for medical devices, including medical device clinical trial design and implementation.

Clinmark’s presentation will include the following topics:
1. Getting approval for a clinical trial
2. Reporting adverse events
3. Independent monitoring aspects
4. Preparing Final Report

Please follow the link to check the event agenda: https://lnkd.in/eMtrYDf Moreover you are cordially invited to visit us at Clinmark’s Stand and explore our offer.