Need to navigate the complexities of the Medical Device Regulation (EU 2017/745)? This is your chance to gain the expertise needed to construct a Technical File and Clinical Evaluation Report โ two critical pillars for regulatory compliance.
Module 2 – Generating Data for Technical Documentation (MDR) begins on May 19, 2025, in collaboration with University of Medicine, Pharmacy, Science and Technology G.E. Palade of Tรขrgu Mureศ.
Why join?
Gain essential knowledge on MDR compliance
Learn from top experts in the field
Elevate your skills to meet regulatory expectations
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๐ฅ๐ฒ๐ด๐ถ๐๐๐ฒ๐ฟ ๐๐ผ๐ฑ๐ฎ๐ ๐ฎ๐ ๐ ๐๐๐.๐ฝ๐ผ๐ฟ๐๐ฎ๐น.๐ป๐ผ๐ฏ๐ผ๐ฐ๐ฎ๐ฝ.๐ฒ๐ โ ๐ก๐ผ๐๐ผ๐๐ฎ๐ฝ ๐๐ผ๐๐ฟ๐๐ฒ๐ โ ๐ฆ๐ฒ๐น๐ฒ๐ฐ๐ ๐ ๐ผ๐ฑ๐๐น๐ฒ ๐ฎ
Register before May 9, 2025.
Donโt miss this opportunity to deepen your regulatory knowledge and stay ahead in the evolving IVD landscape.
