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Upcoming Events

5 October - 13 November 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
Understanding ISO 13485:2016 and the Medical Device Single Audit Programme
3 August - 4 September 2020
Effectively apply a risk-based approach to your biocompatibility studies.
14 September - 16 October 2020, Online Academy
This 5 module course will examine the requirements and design protocols of clinical investigations for new devices with case study examples.
22 - 25 September 2020, New LIVE Online Academy
Regulatory Affairs in Latin America for Medical Devices
5 October - 13 November 2020, Online Academy
Learn about Safety & Security Risk Management, Design Control, Clinical Evaluation and Usability Engineering for Health apps and Medical Device Software
5 - 8 October 2020, New LIVE Online Academy
Understanding labelling and UDI for Medical Devices and IVDs
5 October - 6 November 2020, Online Academy
Understand the EU Regulatory landscape concerning medical software & health apps
7 - 8 October 2020, Radisson Blu Edwardian Kenilworth, London
Successful Medical Device & IVD Post Market Surveillance and Vigilance Reporting
2 - 3 November 2020, Radisson Blu Edwardian Grafton, London
Medical Device Risk Management
10 - 19 November 2020, New LIVE Online Academy
Understand the regulations which directly apply to your product Medical Device Regulation
18 - 19 November 2020, Radisson Blu Edwardian Kenilworth, London
Understanding Clinical Evaluations, Investigations and Post Market Clinical Studies
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.
Dates TBC., Radisson Blu Edwardian Kenilworth, London
Medical Device Regulatory Project Management
Dates TBC, Radisson Blu Royal Hotel, Brussels, Belgium
Advanced Regulatory Affairs for Medical Devices
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
2021 dates TBC., Online Academy
Get to grips with the latest risk management requirements
2021 Dates TBC, 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.
2021 Dates TBC, Radisson Blu Edwardian Kenilworth, London
Understanding Biocompatibility for Medical Devices - The key principles behind, regulations around and common problems which surround biocompatibility
2021 dates TBC, Online Academy
A comprehensive guide on the regulatory requirements necessary for a product's life-cycle within the Russian healthcare industry.
Tailored to your organisation, At a time and place to suit you
Ongoing course

Past Events

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