What is the event about?
The full-day event has been designed for MedTech startups looking to navigate the complexities of MDR, IVDR, QMS, and UKCA.
To help you on the journey to compliance, our experts will provide insights, knowledge and clarity on the regulatory requirements that your products must meet. Throughout the day, you will be given the opportunity to collaborate with other startups and industry peers, and knowledge share with regulatory stakeholders.
If you are a MedTech startup, innovator, product manager or clinical entrepreneur looking to learn more about MDR, IVDR, ISO 13485 and UKCA, this is the event for you.
What will participants gain?
- Guidance on timelines and best practices
- An understanding of the BSI application process and the people you will work with on your way to certification
- Valuable tools that will help with your application
- What to expect on the regulatory journey
Who should attend?
This event has been created to provide insights and learnings for MedTech Startups, innovators, product managers and clinical entrepreneurs embarking on the regulatory pathway to bring products to market.
£50 per person (incl. VAT)
Note: In case of cancellation, the Eventbrite admin fee will still apply.
Take the next step in your MedTech journey. Register here
To find out more about our comprehensive and proven regulatory services, visit our dedicated Medical Devices webpage.
Email: eimeamedical.devicemarketing@bsigroup.com
Phone: +44 345 080 9000
Follow BSI Medical Devices on LinkedIn.
