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Actimed’s work focuses on two primary areas:

  • Helping clients achieve compliance with the Medical Devices Directive 93/42/EEC (incorporating amendments from 2007/47/EC) for the CE marking of medical devices
  • Providing assistance with the design of medical devices on behalf of clients, including design prototyping and sourcing subcontract manufacture where required.


Managing Director, Phil Naylor, is at the forefront of the medical devices industry in a regulatory and quality management capacity. He has over 25 years’ experience in assisting companies to achieve compliance to the regulations and ISO13485 & ISO9001 and has a 100% track record for first-time compliance.


  Actimed's approach

  Actimed believes in taking a direct approach to advising its clients:

  • We get to the core of your business.
  • We are always honest and objective.
  • If something is wrong we will tell you.
  • If something is right we do not tamper with it - it's on to the next stage.
  • We want to see your business prosper as much as you do.


Our work covers many fields and industries including:

  • Sterile Services - SSD, CSSD, TSSU, both private and NHS
  • Medical devices - ranging from surgical instruments to implants (Class I to Class IIb devices)
  • Healthcare – both public service and private hospitals and hospital departments.


See a list of some of our clients and read their recommendations.

Commer House, Station Road, Tadcaster, LS24 9JF, UK
Copyright 2012 Actimed Limited, Registered in England CRO Registered No. 05717254.
Registered Office 9 Systems House, LS24 8LY, UK