LFH Regulatory Limited
Laura Friedl-Hirst is an experienced professional in regulatory affairs, currently serving as the Managing Director and Principal Consultant at LFH Regulatory Limited since June 2019. Previously, Laura held the position of Global Regulatory Affairs Manager at RB for approximately nine months and worked as a Regulatory Affairs Manager at Kapitex Healthcare Limited. Earlier roles include Regulatory Affairs Associate at Thornton & Ross and Regulatory Affairs Specialist at QIAGEN. Laura began a career in regulatory affairs as an Associate at Advanced Medical Solutions and as an IP Student-Regulatory Affairs at DePuy Synthes. Academic qualifications include a Bachelor of Science in Medical Biology and a Foundation degree in Applied Science, both from The University of Huddersfield.
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LFH Regulatory Limited
LFH Regulatory Ltd offers cost-effective regulatory and quality consultancy services by experienced consultants within the Medical Device and In Vitro Diagnostic arena. Our services include; -Device development and CE/UKCA marking certification -Quality Management System Creation and ongoing support to ISO 13485:2016 -Internal/Supplier Audits -Remediating audit findings -Technical documentation -Risk Management activities to ISO 14971 -Clinical requirements -Recalls and Adverse Event management -Product registration -UK Responsible Person Please call us on +44 (0)1484 662575 or email info@lfhregulatory.co.uk for further information.