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Find out about when your SFI agreement will start, what you’re agreeing to do and requesting changes to your agreement.
Comply with good pharmacovigilance practice and prepare for an inspection.
This guide has been provided to reduce the burden when preparing responses to Post Inspection Letters.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
See the list of applications to protect the geographical name of wine and aromatised wine in the UK.
The current conditions affecting boaters on the River Thames and what the warnings mean.
Information you must submit to the Environment Agency in a noise impact assessment that uses computer modelling or spreadsheet calculations.
Your responsibilities as a public body when carrying out or approving works on or near sites of special scientific interest (SSSIs).
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
How to register your chargepoints for OZEV chargepoint grant schemes as a manufacturer.
Imposing safeguard measures for imports of certain steel products.
Advice on writing clear notices and maximising replies to your FSNs.
The efficient and effective undertaking of local plan examinations is heavily reliant on the examination webpages to share information and to assist the Inspector.
How to use a clinical audit to evaluate your digital health product.
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) inspection reports.
Find out how you can process or store similar free circulation goods in place of goods that you have declared to the UK Freeport customs special procedure.
Emerging techniques on how to prevent or minimise the environmental impacts of post-combustion carbon dioxide capture.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
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