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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

  • RP Refresher Training
  • The MHRA’s Guide to Defective Medicinal Products – Part 2
  • The MHRA’s Guide to Defective Medicinal Products – Part 1: Overview

Upcoming Courses

  • Understanding GPhC Guidance for Online Pharmacies – Online Training on 16 March 2026
  • GDP/RP Cogent Gold Standard Online Training on 17 March 2026
  • GDP/RP Cogent Gold Standard WEEKEND Training on 20 March 2026 9:30 am
  • Introduction to Good Distribution Practice Online Training on 20 March 2026 10:00 am
  • RP Forum – tbc on 7 April 2026 10:00 am

MHRA Alerts & Recalls

Class 2 Medicines Recall: Rokshaw Limited Trading as Curaleaf Laboratories, Curaleaf Oil [FS] 10mg/ml THC, 10mg/ml CBD (30ml), EL(26)A/13
12 March 2026
Class 3 Medicines Recall: Bayer Plc, Various Products, EL(26)A/12
12 March 2026
Field Safety Notices: 02 to 06 March 2026
9 March 2026
Class 2 Medicines Recall: Crescent Pharma Limited, Ramipril 5mg capsules, EL(26)A/11
6 March 2026

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