Monir EL AZZOUZI
4 SlideShares 52 Followers 5 Followings
Personal Information
Organization / Workplace
Zürich Area, Switzerland Switzerland
Occupation
Quality and Regulatory Compliance at Johnson & Johnson
Industry
Medical / Health Care / Pharmaceuticals
About
I am a Medical Device expert that want to share his knowledge ans expertise with people that need some support. I am specialized in Quality, Regulatory Compliance and Regulatory Affairs for Medical Devices. On my career I also worked on pharmaceutical products as borderline devices.
Contact Details
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medical devices medical device regulation mdr 2017/745 easy medical device medtech ce marking eu mdr 2017/745 medical device regulations infographic classification eudamed udi ce mark medical device industry prrc quality management system regulatory affairs regulatory compliance pdf free iso 13485 procedures cemark compliance regulatory notified body europe checklist guide agreement authorized representative ear
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Presentations

(2)

Medical Device European Authorized Representative

6 years ago • 20689 Views

Medical device classification following MDR 2017/745

5 years ago • 83525 Views

Documents

(1)

UDI infographic for the Medical Device Regulation

5 years ago • 1658 Views

Infographics

(1)

EU Medical Device Classification MDR 2017/745

6 years ago • 1551 Views

Likes

(1)

UDI infographic for the Medical Device Regulation

Monir EL AZZOUZI • 5 years ago
Personal Information
Organization / Workplace
Zürich Area, Switzerland Switzerland
Occupation
Quality and Regulatory Compliance at Johnson & Johnson
Industry
Medical / Health Care / Pharmaceuticals
About
I am a Medical Device expert that want to share his knowledge ans expertise with people that need some support. I am specialized in Quality, Regulatory Compliance and Regulatory Affairs for Medical Devices. On my career I also worked on pharmaceutical products as borderline devices.
Tags
medical devices medical device regulation mdr 2017/745 easy medical device medtech ce marking eu mdr 2017/745 medical device regulations infographic classification eudamed udi ce mark medical device industry prrc quality management system regulatory affairs regulatory compliance pdf free iso 13485 procedures cemark compliance regulatory notified body europe checklist guide agreement authorized representative ear
See more