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How a marketing authorisation holder should report a defect with a veterinary medicine.
Advice on writing clear notices and maximising replies to your FSNs.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
For MAHs, manufacturers, wholesalers, retailers (including vets) and feed businesses on the manufacture and movement of veterinary medicines in relation to the NI Protocol and Brexit.
Product recall for Aqualung UK Calypso Regulator presenting a serious risk of drowning.
What to do if your vehicle, vehicle part or accessory is recalled, has a registered fault and how to report serious safety defect you find
Get help to classify various types of wood for import and export.
Medicines and Healthcare products Regulatory Agency (MHRA) good manufacturing practice (GMP) deficiencies since April 2010.
This guidance provides an overview of redress measures which ensure that those responsible for contributing to the building safety crisis meet the cost of rectifying their mistakes.
What you need to know about and do to comply with the law and keep consumers safe.
Guidance and forms for recalls and safety defects, download recall data, and issues which could result in a safety issue occurring if they are not fixed.
This study uses microdata on Indian manufacturing plants
Find out when you need to agree a bespoke VAT retail scheme with HMRC.
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