A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK
Much has changed since the Medical Device Regulation (MDR) and the In-Vitro Diagnostic Regulation (IVDR) were adopted in May 2017.
This course will bring you fully up-to-date on:
- the rephrased implementations
- the new guidelines
- role and output from the Medical Device Co-ordination Group (MDCG)
- recent medical device regulatory developments in the UK
It will also consider future developments and the evolving role of the EMA.
This course will provide an excellent opportunity to hear the latest developments from regulatory experts, and enable participants to discuss the implications of the regulations on working practices and the potential impact on future regulatory strategies.
Upcoming start dates
Suitability - Who should attend?
Benefits of attending
This is a must-attend workshop and has been designed for all those working or interested in the medical device and diagnostic market in the EU and the UK.
- Explore the changes in the UK regulation as its system becomes independent and moves away from the EU rules
- Navigate the increasingly complex world of device and diagnostic regulations
- Gain insights into future changes to the regulations and how "digital medicine" may be regulated in the future
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Reviews by course attendees
Average rating 4.8
Very well run, met my objectives, and speakers were interesting, approachable and very knowledgeable.
A relaxed, open forum where you felt comfortable to ask any questions you needed through the presentations and the day. The speakers were all very clear, concise, factual and in...
The speakers were very professional and knowledgeable. They delivered the content in an easy format and allowed plenty of time for questions and interaction from the attendees. ...