As the United Kingdom enters a new era of regulations due to leaving the European Union Templar Regulatory Consulting has been setup to help international medical device companies navigate this new landscape.
Templar Regulatory Consulting can provide UK Responsible Person (UKRP) services to allow international manufacturers legally distribute medical devices, IVDs in the UK. We are also able to provide a range of other services, including training, auditing and consultancy services for medical devices.
Templar Regulatory Consulting can provide UK Responsible Person (UKRP) services to allow international manufacturers legally distribute medical devices, IVDs in the UK. We are also able to provide a range of other services, including training, auditing and consultancy services for medical devices.
Our Services:
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A United Kingdom Responsible Person ("UKRP") is appointed by the company to liase and register their products with the MHRA. Templar Regulatory Consultancy is able to guide and be the UKRP for any international Med Device company wishing to their products in the UK.
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Templar Regulatory Consulting is able to provide specialist for Regulatory Affairs, Quality Management systems, Auditing, Training, GAP Analysis for medical device companies around the world. We are also able to provide training to your staff in order to keep the highest standards at your company.
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