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Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
How to use a quasi-experimental study to evaluate your digital health product.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Use a separate statement of objection form for each Georgian GI product name you object to.
Blogs where government organisations talk about their work and share information and ideas.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Emerging techniques on how to prevent or minimise the environmental impacts of post-combustion carbon dioxide capture.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
A list of 10 criteria that represent good practice in creating, applying and enforcing design codes.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
The CMA is investigating suspected anti-competitive behavior in relation to the supply of fragrances and fragrance ingredients under Chapter I CA98
Find UK trade data from HMRC. Look up data about imports, exports, commodities and traders.
Watch our caseworkers' top tips to make sure your applications are complete and correct. Avoid more than 20 common requisition points.
Legal standards for labelling and composition of food products such as bottled water, milk and meat.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Guidance on promoting the findability of metadata.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Guidance for commissioners and health professionals to make decisions about mental health services and interventions based on data and analysis.
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