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Data, Freedom of Information releases and corporate reports
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
The CMA is consulting on its approach and requirements in the selection, design and implementation of remedies in Phase 1 and Phase 2 merger investigations.
Information about the EU Regulations and their implementation in Northern Ireland
A range of factsheets introducing the work of the Trade Remedies Authority (TRA) and how you can work with us when applying for trade remedies.
This tax information and impact note is about repaying trade remedies duties to businesses, or collecting outstanding duties from businesses, as appropriate.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
How to prepare for implementation and compliance of the Safety Features Regulation.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
This research report evaluates 18 merger remedies put in place by the CC, OFT and the CMA .
The enforcement policy sets out the general principles and approach taken by the Veterinary Medicines Directorate (VMD).
You must get permission to export certain drugs and medicines.
Guidance on applying to register, renew, or vary a Veterinary Homeopathic Remedy.
Find out if anti-dumping duty, countervailing duty and safeguard measures apply to your goods and how to claim a repayment.
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