ISO 14155

With the increasing evidence-based medicine politics, the medical device market is changing. In this interview with Helen Winsor from Pharma IQ , Danielle Giroud, Founder of the World Medical Device Organisation, offers her viewpoint on the direction the market is moving in. She discusses how the regulations.

in the EU compare with those in the US, how they are developing, and the likelihood of eventually having unified global regulations for medical devices.

Giroud offers her perspective on the recent updates to the Medical Device Directive, how it will impact the medical devices industry and what medical device professionals need to do to remain compliant. She also comments on the changes to safety reporting requirements and what challenges these might bring for the industry. Finally, the interview touches upon the new updates within ISO 14155 and how Giroud considers ISO's role within the medical devices industry will develop. Haven’t got the technology to listen to the podcast? Download the transcript here: Keeping a Pace with Changes in Clinical Evaluations for Medical Devices

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ISO 14155

Keeping a Pace with Changes in Clinical Evaluations for Medical Devices

What's Next for the Medical Devices Market? Regulatory Changes

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