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Upcoming Events

8 - 9 December 2020, Radisson Blu Edwardian Grafton, London
Understand the European regulatory landscape for health apps and medical device software from the perspective of two industry experts.
18 - 19 November 2020, Radisson Blu Edwardian Kenilworth, London
Understanding Biocompatibility for Medical Devices - The key principles behind, regulations around and common problems which surround biocompatibility
2 - 5 June 2020, New LIVE Online Academy
Understanding labelling and UDI for Medical Devices and IVDs
2021 dates TBC, Online Academy
A comprehensive guide on the regulatory requirements necessary for a product's life-cycle within the Russian healthcare industry.
2021 dates TBC, Online Academy
This online course will provide an overview of the key regulatory requirements for gaining approvals throughout the MENA region.
Future dates TBC, Online Academy
Decode the new European IVD regulation
Future dates tbc, Online Academy
Familiarise yourself with the latest Medical Device Regulation (MDR) and how it impacts the industry
9 - 18 June 2020, New LIVE Online Academy
Understand the regulations which directly apply to your product Medical Device Regulation
3 August - 4 September 2020, Online Academy
Effectively apply a risk-based approach to your biocompatibility studies.
9 - 18 June 2020, New LIVE Online Academy
Understand the regulations which directly apply to your product Medical Device Regulation
2 - 5 June 2020, New LIVE Online Academy
Understanding labelling and UDI for Medical Devices and IVDs
1 June - 3 July 2020
Get to grips with the latest risk management requirements
6 July - 7 August 2020, 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.
6 July - 7 August 2020, Online Academy
Understand the EU Regulatory landscape concerning medical software & health apps
3 August - 11 September 2020, Online Academy
Learn about Safety & Security Risk Management, Design Control, Clinical Evaluation and Usability Engineering for Health apps and Medical Device Software
3 August - 11 September 2020, Online Academy
Understanding ISO 13485:2016 and the Medical Device Single Audit Programme
1 June - 3 July 2020
This 5 module course will examine the requirements and design protocols of clinical investigations for new devices with case study examples.

Past Events

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