LFH Regulatory is your trusted partner in navigating the complex world of medical device and In Vitro Diagnostic Regulations. 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.
Laura Friedl-Hirst, MD
We take pride in our ability to simplify the regulatory process, ensuring compliance while minimising the burden on our clients. Our experienced consultants have an in-depth knowledge of the intricacies of Medical Device and In Vitro Diagnostic Regulations. We leverage this expertise to guide you through the complexities, saving you time, effort, and stress.
In just four years of trading we grown from strength to strength. This a testament to our dedication and expertise. We have carefully assembled group a of individuals who share our passion for delivering exceptional service and outstanding results. Each team member brings a unique skill set and perspective allowing us to provide comprehensive support across regulatory, quality and clinical solutions.
Jessica Hambidge
At LFH Regulatory we understand that navigating the regulatory landscape can be daunting. That is why we are committed to making the process as smooth as possible for our clients. We work closely with you, offering proactive guidance, transparent communication, and personalised attention at every stage. Your success is our priority, and we are invested in helping you achieve your regulatory and business objectives.
We are proud of the long-term partnerships we have developed with our clients. Our success lies in our ability to deliver results, think creatively and provide unwavering support. By choosing LFH Regulatory you can expect a dedicated team that goes above and beyond to ensure your journey towards compliance is stress-free and successful.
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Our culture is where everyone feels accepted, valued and has a sense of belonging.
We pride ourselves on collaborating with our clients to deliver results, as well as providing safe and effective devices for patients.
We provide an agile and responsive service to ensure we deliver projects to a high standard in a timely manner.
We recognise that a good work/life balance is key for mental and physical wellbeing.
We work with clients and partners to deliver pragmatic and compliant solutions.
We recognise professional development is important for our people, to advise our network with the correct and most up-to-date information
We have a network of trusted partnerships that allows us to deliver an overall work package, taking away the stress of finding cross-functional resources.
We believe in equality and treat each other with respect, regardless of characteristics. This is how we are building a sustainable business.
We are committed to integrity, honesty and openness to deliver the highest standards in our work.
We encourage feedback to allow us to continuously improve everything that we do.
LFH Regulatory is your trusted partner in navigating the complex world of medical device and In Vitro Diagnostic Regulations. Founded in 2019 by Laura Friedl-Hirst, our company has quickly grown into a dynamic team of passionate professionals.
We recognise the critical importance of your QMS to your organisation, customers, patients, and regulatory agencies.
Whether you are navigating the complex UK and European markets or expanding your reach globally, our QMS expertise is tailored to meet your specific needs.
Clinical and performance evaluations are a vital step in validating the safety and efficacy of your medical devices or IVDs.
Understanding Medical Device and In Vitro Diagnostic (IVD) regulations is complex and requires a comprehensive understanding of the entire product lifecycle.
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