Are you a MedTech manufacturer looking to stay ahead in the UK market?
Join this exclusive webinar, hosted by GRS and Med-Di-Dia, to gain expert insights and practical, actionable guidance on the evolving regulatory landscape. Whether you’re focused on medical devices, digital health or in vitro diagnostics, this session will equip you with the knowledge to ensure compliance and market success.
Why Attend?
- Unlock Key Insights: Get a detailed overview of the latest UK medical device regulations and the buzz around CE and UKCA marking.
- Stay Ahead with the Latest Amendments: Stay updated on the progress and development of UK MDR 2002 and understand how they impact your business, ensuring you’re always ahead of the curve.
- Market Access Simplified: Learn about market access requirements for Great Britain and Northern Ireland, including crucial registration and representation obligations.
- Future-Proof Your Business: Explore the future of UK MedTech regulations with a roadmap of upcoming legislative milestones and international recognition routes.
- Embrace Digital Health: Discover evidence requirements for NHS acceptance of Digital Health Technologies.
Who Should Attend?
- MedTech manufacturers
- Regulatory affairs professionals
- Compliance officers
- Quality assurance managers
- Product development teams
Don’t miss this opportunity to stay ahead in the dynamic UK MedTech market. Secure your spot today and ensure your products remain compliant and competitive.
To register your place, please click here.