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Proposed updates to the lists of standards for businesses.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Explains planning controls relating to the storage of hazardous substances in England and how to handle development proposals around hazardous establishments.
Find out what makes a person an enabler of tax avoidance, and what to do about legally privileged communications.
Find out about the rules when a benefit is provided as part of optional remuneration arrangements.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
This guide provides information on statutory derecognition of a trade union
The UK’s consumer connectable product security regime came into effect on 29 April 2024. Businesses in the supply chains of these products now need to be compliant with the legislation.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to work out the VAT on building work and materials if you're a contractor, subcontractor or developer.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Organisational definitions of terms concerned with risk and risk-related matters.
When a material is waste, is a by-product or meets ‘end of waste’ status.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Information for post-16 institutions considering expressing an interest to deliver the first 3 T levels in 2020 to 2021 academic year.
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