Expansion of services at JensonR+

In March, JensonR+ and regenold joined forces to shape our future together.
We are delighted to announce that we are delivering on that commitment. 

Our new Regulatory Manager, Tom Wood will lead the JensonR+ Medical Devices team. Tom joins us from a UK approved/EU Notified body and will be working closely with our sister company CE+ to provide regulatory consultancy and UKRP services to our clients both in the UK and Europe.

We will be offering services in:

  • UK MDR / UKCA

  • EU MDR/IVDR

  • MDSAP

  • ISO 13485

  • UKRP Services

  • Internal Audits

  • Supply Chain Audit

  • Training Services

Tom joins us from DEKRA Certification, where he was a technical assessor in the notified body and UK approved body world, with more than five years of experience, building on his previous medical device manufacturing knowledge.

Tom is looking forward to meeting our current clients and connecting with new clients in the near future.