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MHRA: A guide to defective medicinal products (August 2021)

by Patient Safety Learning

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Summary

The Defective Medicines Report Centre (DMRC) is part of the Medicines and Healthcare products Regulatory Agency (MHRA). The role of the DMRC is to minimise the hazard to patients arising from the distribution of defective medicines by providing an emergency assessment and communication system between manufacturers, distributors, wholesalers, pharmacies, regulatory authorities and users. 

This guide is for patients, healthcare professionals, manufacturers and distributors for reporting, investigating and recalling suspected Defective Medicinal Products.

MHRA: A guide to defective medicinal products (August 2021) https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/1007…
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