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Register to vote Register by 18 June to vote in the General Election on 4 July.
Impact assessment opinions based on external, independent scrutiny of new regulation by the Regulatory Policy Committee.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How test manufacturers or distributors can apply for approval of their tests to sell on the UK market.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
How to prepare and analyse the data you collected for your evaluation.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
This webinar looks at the information an organisation makes available to clients, or potential clients, and how the consumer's expectations can be met.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
These reports set out the Regulator of Social Housing’s approach to consumer regulation.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
What you need to know about and do to comply with the law and keep consumers safe.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
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.
Information for manufacturers.
Things to consider when buying and using products.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Our Assurance products and guidance has been updated. Related guidance and tools are being refreshed and future revised versions will be published on an iterative basis. To ensure you are using the latest versions, you are advised to regularly access...
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