Established in 1994 as GPB Management Consultancy, G.P.B. Limited delivers bespoke, dedicated, effective services to the medical devices and biologics sector by supporting each client fulfil regulatory compliance and quality assurance requirements globally. In partnership with each client we implement solutions via consultancy, training, in-house expertise and provision of advices, including crisis responses, during any stage of a medical device’s life cycle, to meet international quality systems and regulatory standards. We share our expertise with investors requiring product / development diligence pre-investment, clinicians and inventors, research establishments, designers and specification developers, manufacturers, CRO’s for Device / Combination Devices, and Companion Diagnostic Investigations, suppliers importers and contractors, distributors and licensors. We work with clients throughout the EC, US, Canada, Switzerland, Norway, China, Taiwan, Australia, Japan, Brazil, Israel, Brazil and Mexico. GPB have successfully supported our clients complete and maintain market clearance / re-certification of more than 4,000 devices to date.