We are thrilled to introduce two new members of the LFH Regulatory team who bring a wealth of expertise and passion to their roles. Please join us in welcoming Alexander Madell, our new Quality Assurance and Regulatory Affairs Consultant, and Faiza Jabeen, our new Senior Regulatory Affairs Consultant. With their extensive experience and enthusiasm for […]
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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