by Staff | Oct 15, 2020 | Jobs
Clinical Research Associate Clinical Research Associate Key responsibilities: Site management including regular contact with involved site, collecting of essential documents, writing reports, handling of questions, follow-up actions and reporting to 1MED project...
by Staff | Jul 1, 2020 | Free papers, news, Resources
Compared to the old Directives, the new Medical Device Regulation (MDR) reinforces important factors and provides additional requirements concerning the process of clinical evaluation. Since clinical evaluation has always been a major critical activity for medical...
by Staff | Mar 13, 2020 | news
1MED ANNOUNCES MDR DAY 2020 Given the great results achieved during the first edition of the MDR Day in 2019, with more than 30 companies participating in the event, 1MED is happy to announce the second edition of this important gathering. The event will take place in...
by Staff | Feb 20, 2020 | news
TRAINING News 1MED boasts a multi-disciplinary team with expertise in design, engineering and certification of medical devices, combination products (drug-device) and in vitro diagnostics. Given the wide knowledge and experience, our Regulatory Affairs Managers and...
by Staff | Jun 10, 2019 | news
MDR DAY 2019 June 6, 2019 – Milan MDR Day 2019 is the first event organized by 1MED entirely focused on the new European Medical Device Regulation (EU) 2017/745 (MDR). It is dedicated to companies operating in the medical device field, and it welcomes Regulatory...
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