Invibio Ltd
"I’ve had a very positive experience
Any queries have been resolved in a timely manner"
Caroline Prisk
"Working with Psephos Biomedica as our UK Responsible Person (UKRP) has been an exceptional experience. Their team combines deep regulatory expertise with a proactive, solution-oriented approach that has made navigating the UK medical device regulations remarkably smooth and efficient. We highly recommend Psephos Biomedica to any manufacturer seeking a dependable, knowledgeable, and collaborative UKRP partner"
Ammad Shorbaji
Sorimex
"Working with Psephos Biomedica as our UKRP representative in the United Kingdom is smooth and professional. The team responds quickly, supports us with regulatory requirements, and makes the registration of our medical devices on the UK market much easier."
Paweł Sobociński
Ceryx Medical
"We received our letter of no objection from the MHRA! I have to say it was an absolute walk in the park – a couple of requests for extra documents - that was it. That is testament to the quality of the submission that you helped us put together - Thanks loads!"
Stuart Plant
Medentech - part of the Kersia Group
"Medentech Ltd have worked with Psephos as a consultancy partner for our medical device projects since 2021 and we have been very happy to have them work with us on CER preparation and updates since 2022. As part of a small team working on medical device projects in our company, Psephos advice, expertise and knowledge have been extremely valuable to us in this work. I have found them to be professional, efficient and always helpful in all our interactions and would be happy to recommend them to other companies looking for help in this area"