Medical Devices Regulation Webinar

This webinar will inform stakeholder groups on timelines of regulation development and transitional arrangements, following our announcement in October 2022 to extend the current standstill period by 12 months. It will include updates on the regulatory process, the focus groups developing regulatory guidance, and the UK Approved Bodies in place for processing conformity assessments.

Attendees will be informed on regulation development and transitional arrangement timelines; what the MHRA is working on to meet these; how the timelines will affect the work that stakeholders are doing and where to go to ask questions.

This webinar will take place on Tuesday, 24 January 2023, 10:00-11:30 GMT.

Please note registration will close on Thursday 19 January at 11:00.

Programme:

• Future Medical Devices Regulations: overview of current status and future milestones - Penny Wilson, Deputy Director Innovative Devices, MHRA
• The next regulatory milestones in detail: the Statutory Instruments to be laid in Spring 2023 and Summer 2024 - Jillan Hussein, Devices Regulatory Specialist, MHRA
• Developing guidance for the future regulations: an update on the work of 13 focus groups and our commitment to ensure meaningful patient involvement - Catherine Hodgson, Regulatory Affairs Specialist, MHRA
• An update on approved bodies, domestic assurance and supply chain - Suzanne Fuller, Head of Approved Bodies, MHRA

Please note programme is draft and subject to change.

Frequently asked questions

When will I receive details of how to join the meeting?

Once your registration is confirmed, further joining instructions will be sent 48 hours before the meeting. These will include details of how to access the webinar.

How do I cancel my attendance if my plans change?

Email conferences@mhra.gov.uk with the email you used to register attendance and we will cancel your booking.

What platform will the webinar be hosted on?

The webinar will be hosted on GoToWebinar, you will receive further details in your joining instructions.

Access requirements:

We want you to be able to access and participate in the meeting. If you have any access requirements, please let us know when registering.

Meeting recording:

We will be recording this webinar using the GoToWebinar function and plan to make this recording available for public viewing for up to three years on Gov.uk.

Get in touch:

If you have any questions regarding your registration please do get in touch by emailing conferences@mhra.gov.uk.

Data Protection

The Medicines and Healthcare products Regulatory Agency will use the information you have provided via the third-party data processor Eventbrite, to facilitate the event and provide you with an acceptable level of service. Any access requirements will be processed internally and will not be shared in any identifiable way with third-party organisations. We will contact you using the information provided for the purpose of this event.

By providing the information you agree to the data being processed and stored as outlined.

To find out how we use and manage your personal data please visit the MHRA privacy notice.