Tag: Medical Device Development

Industry
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Master MHRA Regulatory Affairs UK

Master MHRA Regulatory Affairs UK

Manage medical devices regulatory activities in the UK

Industry
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Master FDA Regulatory Affairs USA

Master FDA Regulatory Affairs USA

Manage medical devices regulatory activities in the USA

Industry
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Master medical devices registration Levant

Master medical devices registration Levant

Manage medical devices regulatory activities in the Levant market /Be the exper...

Industry
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Master medical devices registration Qatar

Master medical devices registration Qatar

Mater state of Qatar market, by placing your medical devices there, through man...

Industry
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Master medical devices registration in Bahrain

Master medical devices registration in Bahrain

manage medial devices regulatory activities in kingdom of Bahrain market/Be the ...

Industry
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Master medical devices registration Oman

Master medical devices registration Oman

Manage regulatory pathway of medical devices Oman

Industry
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Master Medical Devices Registration Egypt

Master Medical Devices Registration Egypt

Be the expert of medical devices registration in the market of Egypt

Industry
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Master Medical Devices Registration United Arab Emirates

Master Medical Devices Registration United Arab Emirates

Be the expert of placing medical devices in the highly dynamic market of the Uni...

Other Teaching & Academics
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Medical Device Regulation (MDR): Intro for Device Designers

Medical Device Regulation (MDR): Intro for Device Desig...

An introduction to the EU's Medical Device Regulation (MDR) for those involved i...

Industry
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Master Medical Device Registration In Saudi Arabia

Master Medical Device Registration In Saudi Arabia

Master medical devices registration in Saudi Arabia market , the biggest market ...

Software Engineering
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الهندسة الطبية الحيوية وأساسيات صيانة الأجهزة الطبية

الهندسة الطبية الحيوية وأساسيات صيانة الأجهزة الطبية

( هذه الدورة بمثابة دليل نحو تخصص الهندسة الطبية والتعريف بالتحديات التي قد تواج...

Industry
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IVDR 2017 746 regulatory affairs: Learn EU compliance

IVDR 2017 746 regulatory affairs: Learn EU compliance

Understand regulations for Invitro diagnostic medical devices in simple terms to...

Business Law
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Practical Regulatory Affairs 2020 - US FDA Medical Devices

Practical Regulatory Affairs 2020 - US FDA Medical Devices

A practical course discussing the US FDA Medical Device regulations for real-wor...

Business Law
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Practical Regulatory Affairs 2020 - European Medical Devices

Practical Regulatory Affairs 2020 - European Medical De...

A practical course discussing the EU Medical Device Regulation (MDR) in real-wor...

Project Management
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Project Management for Medical Devices

Project Management for Medical Devices

Merging solid project management concepts with medical device development

Business Law
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European Medical Device Regulatory Basics

European Medical Device Regulatory Basics

A beginner's primer to medical device regulation in Europe.

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