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 [email protected] for further information.