By Richard Stubbs
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Decision: Advertising Investigations: October 2025
Decisions made by the MHRA following investigations into complaints about advertising for licensed medicines.
Guidance: International Recognition Procedure
How to use the procedure for medicines licensing applications.
Borderline products: how to tell if your product is a medicine
How the MHRA makes decisions on what is a medicinal product (borderline products).
MHRA Safety Roundup: November 2025
Summary of the latest safety advice for medicines and medical device users
Breast implants – patient perception of risk research
Information for patients, public and healthcare professionals
Class 4 Medicines Defect Notification: Relonchem Ltd, Various Products, EL(25)A/44
Relonchem Ltd has informed the MHRA that duplicate GTIN numbers have been assigned to certain Losartan potassium/Hydrochlorothiazide coated tablets in error and a duplicate EAN number has been assigned to certain Risperidone tablets in error.
