Get your medical device to market quickly & effectively

You’ve made an innovative and life-changing medical device or IVD that the market needs. The next step, is navigating the ever-changing world of regulation and getting it to market. Our agile team of experts can guide and support you with consultancy, regulatory documentation writing, UKRP, quality management & more.

64+

Years Experience

Agile

Team

Experts

We’re specialists in regulation

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How we can help you

No matter what you need support with, our range of services can support you right from product inception through to post-market monitoring, helping you have a cohesive system that gets your product to market and keeps it there. Our services:

About Us

Founded in 2019 by Laura Friedl-Hirst, our company has quickly grown into a dynamic team of passionate professionals. Together, we work closely with our clients to make the process of regulation and compliance as stress-free as possible. 

What truly sets LFH Regulatory apart is our commitment to building strong, long term relationships with our clients. We believe that collaboration and open communication are vital in understanding your unique challenges and goals. By working closely with your business and product, we can provide tailored solutions that remove the stress from Medical Device Regulation and In Vitro Diagnostic Regulation.

The team that will be supporting you:

Laura Friedl-Hirst

Managing Director & Principal Consultant

Helen George

Business Manager

Jessica Hambridge

Head of Regulatory Affairs

Ellie Shackleton

Clinical & Regulatory Consultant

Dr Yupei Xiao

Clinical & Regulatory Consultant

Josephine Shonaike

Medical Writer

Hayley Barwick

Senior Quality Assurance and Regulatory Affairs Consultant

Lydon Boyer

Quality Assurance and Regulatory Affairs Consultant