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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.
Guidance on labelling for medicinal products used in clinical trials.
Guidance for clinical trials that use Decentralised Manufactured Investigational Medicinal Products (IMPs).
Guidance on using non-investigational medicinal products in a clinical trial.
Guidance on clinical trials that are categorised as ‘notifiable’.
The Independent Monitoring Authority for the Citizens’ Rights Agreements (IMA) will work to protect the rights of EU and EEA EFTA (Iceland, Liechtenstein and Norway) citizens in the UK and Gibraltar. IMA is an executive non-departmental public body, sponsored by...
We provide independent panels that review suitability to adopt or foster and other decisions made by adoption and fostering providers. IRM works with the Department for Education .
Protected wine name with Protected Geographical Indication (PGI)
The eMIT provides information about prices and usage for generic drugs and pharmaceutical products.
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