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MHRA, U.K. Road Map and Swiss Regulatory Updates

In this webinar, an Emergo by UL subject matter expert outlines the latest updates about U.K. MHRA and Switzerland medical device regulations.

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Watch now: MHRA, U.K. road map and Swiss regulatory updates

The Medicine and Healthcare products Regulatory Agency (MHRA) issued a response on the future regulations in the U.K. on June 26, 2022. The responses are intended to help medical device manufacturers understand the MHRA’s position on the future legislation. This outlines the road map and some of the strategic regulatory comments about the future legislation provided by MHRA. 

Webinar date 

Jan. 31, 2023


Karen Hill, senior consultant, Regulatory Affairs, Emergo by UL


This webinar will help you gain a better understanding of the regulatory strategy decisions they might consider regarding compliance in the U.K. You will learn practical information intended to equip manufacturers for future medical device marketing submissions.

Learning objectives:
  • Strategic regulatory comments about the future legislation provided by MHRA.
  • Updates about the latest regulations for medical devices in Switzerland.
About the presenter

Karen Hill, senior consultant, Regulatory Affairs, Emergo by UL

Karen Hill has over 20 years of Medical Device industry experience, primarily focused on high-risk, implantable devices and In Vitro Diagnostics (IVDs). Hill’s background includes extensive experience in EU activities, such as Technical File/Design Dossier preparation, Clinical Evaluation Reports and change notifications. She is one of Emergo’s leading consultants for support with European Medical Device/IVD Regulatory changes. On top of her European regulatory expertise, Hill has also cleared multiple FDA 510(k)s and has several years of global regulatory research and strategy experience.


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