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Upcoming Events

1 - 27 October 2019, Online Academy
Effectively apply a risk-based approach to your biocompatibility studies.
4 November - 6 December 2019, Online Academy
Understanding ISO 13485:2016 - Online Academy
20 - 21 November 2019, Radisson Blu Edwardian Grafton, London
Understanding Biocompatibility for Medical Devices - The key principles behind, regulations around and common problems which surround biocompatibility
12 June 2019, Webinar
Gain an updated understanding of the implications Brexit will pose on the Medical Device Industry
26 - 27 June 2019, Radisson Blu Edwardian Grafton, London
Medical Device Risk Management
Starts 1 July 2019, Online Academy
Decode the new European IVD regulation
Next intake begins 1 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 - 28 July 2019, Online Academy
Get to grips with the latest risk management requirements
8 - 9 July 2019, Radisson Blu Edwardian Kenilworth, London
Medical Device Regulatory Project Management
15 - 16 July 2019, Radisson Blu Edwardian Grafton, London
Successful Medical Device & IVD Post Market Surveillance and Vigilance Reporting
Next intake begins 1 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.
16 - 17 September 2019, Hotel Berlin, Berlin
Understand the regulations which directly apply to your product Medical Device Regulation
18 - 19 September 2019, Hotel Berlin, Berlin
Advanced Regulatory Affairs for Medical Devices
8 - 9 July 2019, Radisson Blu Edwardian Kenilworth, London
Medical Device Regulatory Project Management
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.
Next intake begins 1 October 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.
Next intake begins 1 October 2019, Online Academy
This online course will provide an overview of the key regulatory requirements for gaining approvals throughout the MENA region.
1 - 27 October 2019, Online Academy
Effectively apply a risk-based approach to your biocompatibility studies.
1 October - 3 November 2019, Online Academy
Familiarise yourself with the latest Medical Device Regulation (MDR) and how it impacts the industry
1 - 28 July 2019, Online Academy
Get to grips with the latest risk management requirements
21 - 22 October 2019, Radisson Blu Edwardian Kenilworth, London
Understanding the European IVD Regulation
15 - 16 July 2019, Radisson Blu Edwardian Grafton, London
Successful Medical Device & IVD Post Market Surveillance and Vigilance Reporting
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.
Starts 1 July 2019, Online Academy
Decode the new European IVD regulation
1 - 28 July 2019, Online Academy
Understand the EU Regulatory landscape concerning medical software & health apps
4 November - 6 December 2019, Online Academy
Understanding ISO 13485:2016 - Online Academy
3-week online course | Starts 4 November 2019, Online Academy
3-week online course | 2 hours per week
11 - 12 November 2019, Radisson Blu Edwardian Kenilworth, London
Understanding Clinical Evaluations, Investigations and Post Market Clinical Studies
12 - 14 November 2019, Radisson Blu Edwardian Grafton, London
Medical Device School
26 - 27 June 2019, Radisson Blu Edwardian Grafton, London
Medical Device Risk Management
20 - 21 November 2019, Radisson Blu Edwardian Grafton, London
Understanding Biocompatibility for Medical Devices - The key principles behind, regulations around and common problems which surround biocompatibility
27 - 28 November 2019, Radisson Blu Edwardian Grafton, London
US Regulatory Affairs for Medical Devices
2 - 3 December 2019, Grand Hotel Bohemia, Prague
Gaining Marketing Authorisation in the CIS for Medical Devices
TBC 2020, Radisson Blu Edwardian Grafton, London
Regulatory Affairs in Latin America for Medical Devices
Tailored to your organisation, At a time and place to suit you
Ongoing course

Past Events

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