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Medical Device Consultancy

Medical Device Consultancy

by John Finey | Oct 23, 2023 | Blog, Consultancy, Medical Devices, Training

We are delighted to launch an updated Medical Device training and consultancy offering.

Medical Devices – the picture is still clear as mud!

Medical Devices – the picture is still clear as mud!

by John Finey | Aug 30, 2023 | Blog, Medical Devices

Let’s throw in some more cliches, there are still many plates spinning, balls in the air and how long is a piece of string?

Medical Devices – Consultation on the future regulation of medical devices in the United Kingdom

Medical Devices – Consultation on the future regulation of medical devices in the United Kingdom

by Steven Hewison | Jun 27, 2022 | Blog, Medical Devices

Following the UK’s exit from the European Union (EU), the government identified a unique opportunity to improve how medical devices and in vitro diagnostic medical devices (IVDs) are regulated in the United Kingdom.

The Future of Medical Device Regulation

The Future of Medical Device Regulation

by Steven Hewison | Oct 25, 2021 | Blog, Medical Devices

The Future of Medical Device Regulation in the UK- Do you know that the regulatory framework for the manufacture and supply of medical devices in the UK is changing?

The Future of Medical Device Regulation

The Future of Medical Device Regulation

by Amelia Holmes | Sep 27, 2021 | Blog, Medical Devices, MHRA, Regulation

The Future of Medical Device Regulation, on the 16th of September, the Medicines and Healthcare products Regulatory Agency (MHRA) launched a 10- week

Deadline Approaching – Medical Device Registration

Deadline Approaching – Medical Device Registration

by John Finey | Aug 19, 2021 | Blog, Medical Devices, MHRA

Deadline approaching – Medical Device Registration for registering Class IIa and Class IIb (other than implants) products with the MHRA is the end of August 2021.

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Recent Posts

  • MHRA-NICE aligned pathway
  • New regulations for clinical trials
  • Pharmacy Consulting Ltd – Audit Training

Upcoming Courses

  • Introduction to Good Distribution Practice Online Training on 10 April 2026 10:00 am
  • Intro to the Responsible Person (import) Role (Online) on 13 April 2026
  • GDP/RP Cogent Gold Standard Online Training on 14 April 2026
  • Active Pharmaceutical Ingredient (API) and Clinical Trials Online Training on 27 April 2026 2:00 pm
  • Introduction to Good Distribution Practice Online Training on 13 May 2026 10:00 am

MHRA Alerts & Recalls

Field Safety Notices: 30 March - 3 April 2026
8 April 2026
MHRA Safety Roundup: March 2026
31 March 2026
Field Safety Notices: 23-27 March 2026
31 March 2026
Class 2 Medicines Recall: Bio Products Laboratory Limited, Rabies, Human normal Immunoglobulin 500IU solution for Injection, EL(26)A/18
30 March 2026

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Hampshire
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