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Upcoming Events

1 April - 13 May 2019, Online Academy
A comprehensive course for professionals who are involved in clinical investigations and post market clinical follow-up studies - study online at your own pace.
7 May - 9 July 2019, Online Academy
This flexible online course offers students an excellent opportunity to understand the entire medical device product lifecycle in the context of regulatory updates under the MDR.
1 - 19 April 2019, Online Academy
3-week online course | 2 hours per week
7 May - 17 June 2019, Online Academy
Understanding ISO 13485:2016 - Online Academy
1 April - 6 May 2019, Online Academy
This online course will provide an overview of the key regulatory requirements for gaining approvals throughout the MENA region.
1 April - 6 May 2019, Online Academy
This online course will provide an overview of the key regulatory requirements for gaining approvals throughout the MENA region.
1 - 19 April 2019, Online Academy
3-week online course | 2 hours per week
7 May - 9 July 2019, Online Academy
This flexible online course offers students an excellent opportunity to understand the entire medical device product lifecycle in the context of regulatory updates under the MDR.
7 May - 17 June 2019, Online Academy
Understanding ISO 13485:2016 - Online Academy
1 April - 13 May 2019, Online Academy
A comprehensive course for professionals who are involved in clinical investigations and post market clinical follow-up studies - study online at your own pace.
26 - 27 June 2019, Radisson Blu Edwardian Grafton, London
Medical Device Risk Management
21 - 22 May 2019, Radisson Blu Edwardian Grafton, London
Understanding Biocompatibility for Medical Devices - The key principles behind, regulations around and common problems which surround biocompatibility
1 - 28 July 2019, Online Academy
Get to grips with the latest risk management requirements
12 - 14 November 2019, Radisson Blu Edwardian Grafton, London
Medical Device School
3-week online course | Starts 4 November 2019, Online Academy
Overcome regulatory challenges by learning best-practices for developing user-friendly and effective health apps and software.
1 - 28 July 2019, Online Academy
Understand the EU Regulatory landscape concerning medical software & health apps
7 May - 2 June 2019, Online Academy
Effectively apply a risk-based approach to your biocompatibility studies.
1 July - 3 August 2019, Online Academy
Decode the new European IVD regulation
8 - 9 May 2019, Radisson Blu Edwardian Grafton, London
Understanding Clinical Evaluations, Investigations and Post Market Clinical Studies
7 May - 9 June 2019, Online Academy
Familiarise yourself with the latest Medical Device Regulation (MDR) and how it impacts the industry
1 July - 3 August 2019, Online Academy
Decode the new European IVD regulation
26 - 27 June 2019, Radisson Blu Edwardian Grafton, London
Medical Device Risk Management
21 - 22 May 2019, Radisson Blu Edwardian Grafton, London
Understanding Biocompatibility for Medical Devices - The key principles behind, regulations around and common problems which surround biocompatibility
8 - 9 May 2019, Radisson Blu Edwardian Grafton, London
Understanding Clinical Evaluations, Investigations and Post Market Clinical Studies
1 - 28 July 2019, Online Academy
Get to grips with the latest risk management requirements
1 - 28 July 2019, Online Academy
This 5 module course will examine the requirements and design protocols of clinical investigations for new devices with case study examples.
7 May - 2 June 2019, Online Academy
Effectively apply a risk-based approach to your biocompatibility studies.
7 May - 9 June 2019, Online Academy
Familiarise yourself with the latest Medical Device Regulation (MDR) and how it impacts the industry
1 - 28 July 2019, Online Academy
This 5 module course will examine the requirements and design protocols of clinical investigations for new devices with case study examples.
1 - 28 July 2019, Online Academy
Understand the EU Regulatory landscape concerning medical software & health apps
1 October - 5 November 2019, Online Academy
A comprehensive guide on the regulatory requirements necessary for a product's life-cycle within the Russian healthcare industry.

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