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MHRA Safety Features Team

by Jackie (née Heneghan) Peck | Apr 3, 2017 | Blog, Falsified Medicines, MHRA, Regulation, WDA(H)

The Safety Features Team have set up a mail box for queries you might have regarding the new FMD requiring the registering of products onto the new EMVO portal:

[email protected]

← Flu Vaccination claims What is EMVO? →

Recent Posts

  • Considerations for Quality Agreements
  • GDP certificates do not expire
  • Parallel Trade – A reminder

Upcoming Courses

  • Licence Holder Training on 10 June 2025 10:00 am
  • GDP/RP Cogent Gold Standard Online Training on 17 June 2025
  • RP Forum – Inspection Preparation and RP Readiness on 8 July 2025 10:00 am
  • GDP Audit Online Training on 9 July 2025 10:00 am
  • GDP/RP Cogent Gold Standard Online Training on 15 July 2025

MHRA Alerts & Recalls

Field Safety Notices: 26 to 30 May 2025
3 June 2025
Class 4 Medicines Notification, Zentiva Pharma UK Limited, Various Products, EL(25)A/24
2 June 2025
Philips Respironics BiPAP A series ventilators: alarm malfunction and risk of therapy interruptions in ventilators not intended for life-support, DSI/2024/006
23 May 2025
Class 2 Medicines Recall: Mercaptopurine 50mg Tablets, Aspen Pharma Trading Limited, EL (25)A/23
22 May 2025

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Wellesley House
10 Eelmoor Road
Farnborough
Hampshire
GU14 7QN

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