Events

Together, we will tackle the ever- evolving opportunities and challenges for our industry, from innovation and digital transformation to regulatory developments and sustainability.

This event will offer a unique platform for exploring the latest in regulatory guidance, including updates from the FDA's 2022 draft guidance on human factors.

The summit focuses on partnerships, licensing deals, and innovation in drug development.

This seminar offers essential guidance on effectively utilizing the ISO 10993 standards and integrating a robust risk management approach into the biological evaluation process of medical devices.

You hear the latest research discoveries from the experts, learn about technology advances in the field, participate in panel discussions and poster presentations, and build new network.

Our six-in-one design and manufacturing expo is designed to give you a comprehensive view of the product lifecycle—from prototype to production.

It focuses on fostering strategic partnerships, licensing opportunities, and collaborations to drive innovation in drug development and bring new therapies to market.

The programme of the 5th GFMD, will consider sessions on: Selection of Priority Medical Devices, Medical Devices information system, Essential in vitro diagnostics, innovation, regulation, health technology assessment for medical devices, health technology management

With presentations and panel discussions on industry trends and outsourcing challenges, this 2-day event is a must-attend for the medical device and diagnostics community.

This event offers valuable insights and tactics to enhance the professional growth of executives engaged in medical device aspects.