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Acorn Regulatory Conducting Internal Audits

Conducting Internal Audits – Guidance from our Quality Team

Our quality team has a well deserved reputation for excellence.  In this blog they share their thoughts on what you need […]

EU Medical Device Vigilance Reporting - Part 1 - 'The Abridged Guide' - Acorn Regulatory

EU Medical Device Vigilance Reporting: Part 2 – Frequently Asked Questions

  In part 1 of this series we gave you a quick overview of the medical device vigilance reporting requirements for IVD […]

EU Medical Device Vigilance Reporting - Part 1 - 'The Abridged Guide' - Acorn Regulatory

EU Medical Device Vigilance Reporting – Part 1 – ‘The Abridged Guide’

If you are a manufacturer of an IVD or a medical device, once your product is on the market, you […]

CE Marking An App

Do You Want To Find Out About CE Marking An App? Find Out More Here

There has been a veritable explosion in the number of mobile apps which act as aids to patients and clinicians […]

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New European Medical Device and IVD Regulation – Where is it?

The long anticipated wait for agreement and adoption of the new European Medical Device and IVD Regulations will go on […]

In Vitro Diagnostic Medical Device Regulations Acorn Regulatory

Borderline Medical Devices Covered in EU Manual Update

With the rapid development of new software tools and mobile apps in healthcare, questions arising over classification will become increasingly […]

Contact us and enjoy a faster, smoother journey through the maze of European Pharmaceutical and Medical Device legislation with us as your expert guide.
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