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Calls For More Patient Input In Medical Device Development And Regulation

 
• By Eliza Slawther

It is vital to involve patients in medical device development, regulatory assessments, and post-marketing activities. The European Patients’ Academy on Therapeutic Innovation (EUPATI) has explained why and what it is doing to drive progress.

Patient Input
• Source: Shutterstock

A new roadmap providing a guideline for how patient engagement can bolster each step of the medical device life cycle and prevent problems from arising later on was presented at a recent EUPATI open webinar.

Dominique Hamerlijnck, a patient advocate and EUPATI fellow explained that this is a “concept” roadmap at present; The impact of...

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Long-Awaited EUDAMED Notice Ushers In New Era Of Compliance

 
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Proposed Revision Of Digital Rules – EU’s Good Start But Medtech Advises Caution

 
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How The EU’s Digital Omnibus Package Could Provide Breathing Space For Medtech

 
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The European Commission seems to have heeded many of the medtech industry’s points regarding challenges with the implementation of the AI Act within the Digital Omnibus. But the usual EU hurdles must be crossed before the sector will know if these proposals will make it into law.

More from Geography

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What Exact-ly Is In Store For Liquid Biopsy?

 
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LDTs Aimed At Catching Cancers Early Hold Promise In Reducing Late-Stage Diagnoses, Study Shows

 
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A recent study demonstrates that certain types of blood-based tests that screen for multiple cancers at once have the potential to flip the script on cancer diagnoses, including some of the deadliest types.

How The EU’s Digital Omnibus Package Could Provide Breathing Space For Medtech

 
• By Amanda Maxwell

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