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This guide has been provided to reduce the burden when preparing responses to Post Inspection Letters.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Advice for medical professionals to use when assessing drivers with cardiovascular disorders.
Common user charge rates and how the charge applies to imports entering Great Britain through the Port of Dover and Eurotunnel.
Information from the National Health Service on conditions, treatments, local services and healthy living
Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Understand and avoid all types of anti-competitive and cartel activity including price-fixing, collusion, bid-ridding and sharing markets. Know how to report concerns to the CMA.
Check the tariff classification for a defined daily dose of active substances.
Advises on how planning can manage potential noise impacts in new development.
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) inspection reports.
Find out if the goods you're declaring to inward or outward processing are classed as sensitive goods.
Use a separate statement of objection form for each Japanese GI product name you object to.
The CMA investigated alleged excessive and unfair pricing, anti-competitive agreements and abusive conduct with respect to hydrocortisone tablets under Chapters I and II CA98 and Articles 101 and 102 TFEU.
Argentina is subject to transit control for military goods and restrictions for controlled goods and technology.
This guidance describes case definitions to inform testing and reporting of suspected mpox cases.
Complete Self-Assessment form F3 or F3(S) for proposed, new and upgraded CHP Schemes
Check the tariff classification for saltwater fish.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
Guidance and recommendations from the Committee on Mutagenicity of Chemicals in Food, Consumer Products and the Environment (COM).
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