What’s your approach to meeting EU MDR Article 117?

A review of the challenges in the complex area of GSPR and how to achieve compliance

Welcome to MediPhorum

The power of collaboration…
advancing medical technology for all.

BioPhorum is where the global biopharmaceutical and device industries can collaborate and accelerate progress – for the benefit of all.

MediPhorum is built on BioPhorum’s proven collaboration model to bring members invaluable access to industry advancements,
regulatory bodies, thought leadership and best practices. By providing a safe and trusted space for industry pioneers to exchange insights and share expertise. MediPhorum aims to drive the development of cutting-edge solutions that will ultimately reshape the future of healthcare. Be part of this growing community.

Discover the great benefits you’ll enjoy as a MediPhorum member

An open and safe environment to facilitate industry wide collaboration in medical technology.

Being a part of MediPhorum makes you part of an experienced growing community of great minds. Our dedicated facilitators orchestrate collaborations that focus targeted medical technology segments to develop new ways of doing things. Being a part of MediPhorum doesn’t only support world efforts for improving medical technology it grows our combined technical expertise.

A community connecting with a cause.

More minds collaborating are better than one.

Accelerating development and performance.

Are you ready to become a member? Make an enquiry today.

MediPhorum success stories

Facing one of the most significant MedTech regulatory challenges over the last 20 years, the EU MDD to MDR transition, MediPhorum members collaborated to streamline the submission processes for their first and subsequent Notified Body Opinions, reducing the number of clarification questions received

Implementation of Article 117 of European Union Medical Devices Regulation (EU MDR) General Safety and Performance Requirements: a position paper
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MediPhorum members are collaborating to build an aligned guidance / best practice approach that will be shared with regulators to build a common understanding and harmonized approach helping to reduce time to market.

Human Factors industry opinion survey: ​US submissions for drug delivery devices
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Kickstart your career with MediPhorum

Bringing together the brightest minds in the medical technology industry.

Are you are the catalyst who energizes industry-changing breakthroughs, nurtures creative solutions and empowers the industry to achieve real outcomes?

We want you to join our team.