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The MDTI Knowledge Hub
Explore insights, analysis and expertise from MDTI trainers
Webinars and interviews for the medical device industry
In this interview with Richard Young, trainer for Understanding ISO 13485:2016, he takes us through the 2016 revision of the standard, and how it affects the medical device industry.
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. Read the interview.
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. Read the interview.
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.
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.
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.
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.
In this webinar, Richard Young talks through valuable updates and insights into the classification system proposed in the new IVD regulation. Watch the webinar.