G.P.B. Limited provides bespoke, dedicated services to support each Client fulfil and maintain regulatory compliance and quality assurance requirements. In partnership we design best fit strategies, implement effective and efficient business focused controls to meet national and/or global standards that enable and sustain market clearance.
In partnership we implement solutions via consultancy, training, in-house expertise and provision of advices, including crisis responses, during any stage of our Client’s medical devices’ life cycle, to meet national or international quality systems and regulation. We share our expertise with investors requiring due diligence / re-investment, clinicians and inventors, research establishments, designers and specification developers, manufacturers, CRO’s for Device Investigations, suppliers, importers, contract manufacturers, distributors and licensors.
GPB continue to work with clients throughout the EC, US, Canada, Switzerland, Norway, China, Taiwan, Australia, Japan, Brazil, Israel, and Mexico and have successfully supported our clients implement and maintain some 100+ management systems and attain market clearance / re-certification of 4,000 + devices to date.
George Buchan, Founder and Managing Director of G.P.B. Limited
Provide innovative, responsive, consulting, training and support services that deliver value to each Client’s organisation and enterprise
Engage and partner with experienced, professional associates and organisations to deliver a broad range of practical, efficient, quality improvement and compliance solutions
Develop and apply our expertise with diligence, consideration, enthusiasm, openness and integrity
Deliver what we promise to ensure Client satisfaction
Maintain ethical standards of professional conduct
Remain profitable to invest and grow