Monir EL AZZOUZI
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Personal Information
Organização/Local de trabalho
Zürich Area, Switzerland Switzerland
Cargo
Quality and Regulatory Compliance at Johnson & Johnson
Setor
Medical / Health Care / Pharmaceuticals
Sobre
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.
Detalhes do contato
Marcadores
medical devices medical device regulation mdr 2017/745 medtech easy medical device ce marking regulations infographic classification medical device eu mdr 2017/745 checklist europe notified body guide agreement authorized representative ear regulatory compliance cemark procedures iso 13485 free pdf regulatory compliance regulatory affairs quality management system prrc medical device industry ce mark udi eudamed
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Apresentações

(2)

Medical Device European Authorized Representative

Há 7 anos • 21530 Visualizações

Medical device classification following MDR 2017/745

Há 7 anos • 85424 Visualizações

Documentos

(1)

UDI infographic for the Medical Device Regulation

Há 6 anos • 1693 Visualizações

Infográficos

(1)

EU Medical Device Classification MDR 2017/745

Há 7 anos • 1789 Visualizações

Gostaram

(1)

UDI infographic for the Medical Device Regulation

Monir EL AZZOUZI • Há 6 anos
Personal Information
Organização/Local de trabalho
Zürich Area, Switzerland Switzerland
Cargo
Quality and Regulatory Compliance at Johnson & Johnson
Setor
Medical / Health Care / Pharmaceuticals
Sobre
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.
Marcadores
medical devices medical device regulation mdr 2017/745 medtech easy medical device ce marking regulations infographic classification medical device eu mdr 2017/745 checklist europe notified body guide agreement authorized representative ear regulatory compliance cemark procedures iso 13485 free pdf regulatory compliance regulatory affairs quality management system prrc medical device industry ce mark udi eudamed
Ver mais