MDTI is part of the Knowledge & Networking Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

Informa

Upcoming Events

4 - 29 November 2019, Online Academy
Understand the EU Regulatory landscape concerning medical software & health apps
4 November - 16 December 2019, Online Academy
Understanding ISO 13485:2016 and the Medical Device Single Audit Programme
3-week online course | Starts 4 November 2019, Online Academy
3-week online course | 2 hours per week
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.
12 - 14 November 2019, Radisson Blu Edwardian Grafton, London
Medical Device School
18 - 19 November 2019, Radisson Blu Edwardian Kenilworth, London
Medical Device Risk Management
TBC 2020, Radisson Blu Edwardian Grafton, London
Regulatory Affairs in Latin America for Medical Devices
2 - 3 December 2019, Le Palais Art Hotel Prague
Gaining Marketing Authorisation in the CIS for Medical Devices
27 - 28 November 2019, Radisson Blu Edwardian Grafton, London
US Regulatory Affairs for Medical Devices
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
16 - 17 September 2019, Hotel Berlin, Berlin
Understand the regulations which directly apply to your product Medical Device Regulation
23 - 24 October 2019, Radisson Blu Edwardian Grafton, London
Successful Medical Device & IVD Post Market Surveillance and Vigilance Reporting
25 - 26 September 2019, Radisson Blu Edwardian Kenilworth, London
Medical Device Regulatory Project Management
18 - 19 September 2019, Hotel Berlin, Berlin
Advanced Regulatory Affairs for Medical Devices
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.
Starts 1 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 - 27 October 2019, Online Academy
Get to grips with the latest risk management requirements
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.
Tailored to your organisation, At a time and place to suit you
Ongoing course
Next intake begins 16 September 2019, Online Academy
This 5 module course will examine the requirements and design protocols of clinical investigations for new devices with case study examples.
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.
21 - 22 October 2019, Radisson Blu Edwardian Kenilworth, London
Understanding the European IVD Regulation
11 - 12 November 2019, Radisson Blu Edwardian Kenilworth, London
Understanding Clinical Evaluations, Investigations and Post Market Clinical Studies

Past Events

There are no matching events to show.