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Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
What detailed information you need to send to HMRC to support your Research and Development (R&D) tax relief claim, and when and how to submit it.
Get help to classify articles of leather and other items in chapter 42 of the tariff for import and export.
Subject matter specialists provide invaluable advice to Ofqual as we carry out our role in regulating qualifications. Find out how to apply to be one.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
This study traces the impact of these systematic reviews by looking at use within government and other organisations
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How data on landings statistics are collected and processed by fisheries administrations in the UK.
Actions that trial sponsors should consider to build resilience into clinical trial design
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Guidelines for civil panel counsel, revised to include the new government security classifications.
DFID rapid evidence assessments provide rigorous and policy relevant syntheses of evidence, carried out in 3-6 months.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
How to use A/B testing to evaluate your digital health product.
Join us as a Research Officer to launch a brilliant career in Government Social Research.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
How to use a contextual inquiry when developing your digital health product.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
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