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The MDTI Knowledge Hub


resources introduction to regulatory affairs for medical devices anne jury

In this interview with Anne Jury, we take a look at the implications of the new MDR and how it will affect professionals within the medical device industry. Anne Jury, the trainer for MDTI’s upcoming course Introduction to Regulatory Affairs for Medical Devices, will advise on how to prepare for the MDR and maintain compliance.
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resources medical device school barry fitch

In this interview Barry Fitch, one of the trainers for MDTI’s leading course Medical Device School, takes us through the challenges that medical device professionals currently face with the new MDR and the IVDR. Barry gives us an insight into how professionals can best prepare for these changes, as well as how his section of the course will benefit attendees.
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resources medical device school howard dobbs

Howard Dobbs, one of the course trainers for MDTI’s leading course Medical Device School, advises on how the regulatory changes will affect medical device professionals, and what they can do to prepare for it. Howard also takes us through why the Medical Device School is valuable for those within the field. 
Read the interview.


resources navigating pricing and the reimbursement landscape in europe 1

In this webinar with Emmanuel Garnier (Solicitor at Simmons & Simmons), he talks us through the pricing and reimbursement strategies available in France, German and the UK. Watch the webinar.


Richard Young leads this webinar, exploring a major area of development within the industry. Richard addresses the regulatory environments and key standards to be aware of. Watch the webinar.

resources iso 13485 2016 an overview of general and product realisation requirements 1

This webinar, led by Richard Young, covers the impacts of the new revision including new terminology, general requirements, design controls and resource management. Watch the webinar.

clinical evaluations incorporating biological evaluation and pmcf with sam martin

In this webinar, Sam Martin gives us an overview of clinical evaluation and how it interacts with biological evaluations and port market clinical follow-up. Watch the webinar.

resources future european regulation of in vitro classification

In this webinar, Richard Young talks through valuable updates and insights into the classification system proposed in the new IVD regulation. Watch the webinar.

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