News & Events
1MED INNOVATION DIGITAL FORUM
Il 3 Luglio si è tenuto il primo 1MED INNOVATION DIGITAL FORUM, un incontro virtuale che ha permesso di approfondire temi di attualità relativi alla prossima applicazione del Nuovo Regolamento sui Dispositivi Medici (UE) 2017/745 e del Nuovo Regolamento sulla...
Clinical data and clinical evidence requirements under MDR: free Expert Guidance
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...
26 MAY 2021: the new Date of Application of MDR
In order to prioritise focus of Member States, health institutions and economic operators on the fight against COVID-19 pandemic, the European Parliament and the Council has today approved to postpone the Date of Application (DoA) of the Medical Device Regulation (EU)...
1MED ANNOUNCES MDR DAY 2020
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...
TRAINING
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...
MDR DAY 2019
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 and...
News & Events
1MED INNOVATION DIGITAL FORUM
Il 3 Luglio si è tenuto il primo 1MED INNOVATION DIGITAL FORUM, un incontro virtuale che ha permesso di approfondire temi di attualità relativi alla prossima applicazione del Nuovo Regolamento sui Dispositivi Medici (UE) 2017/745 e del Nuovo Regolamento sulla...
Clinical data and clinical evidence requirements under MDR: free Expert Guidance
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...
26 MAY 2021: the new Date of Application of MDR
In order to prioritise focus of Member States, health institutions and economic operators on the fight against COVID-19 pandemic, the European Parliament and the Council has today approved to postpone the Date of Application (DoA) of the Medical Device Regulation (EU)...
1MED ANNOUNCES MDR DAY 2020
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...
TRAINING
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...
MDR DAY 2019
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 and...