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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Employment Appeal Tribunal Judgment of Mr Justice Sheldon on 19 August 2025.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Explainers relating to the Northern Ireland Troubles (Legacy and Reconciliation) Bill
Guidance on conditional marketing authorisations, exceptional circumstances marketing authorisations and national scientific advice.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
Distinguishes randomised controlled trials from other types of study within research papers to help NICE staff narrow down the number of papers they need to read and review for evidence synthesis.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
Guidance for Applicants wishing to apply for a Promising Innovative Medicines designation, pre-submission meeting or an EAMS Scientific Opinion.
Information on comparator products used in studies supporting abridged marketing authorisation application.
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