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.

LFH Regulatory Limited

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