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Guidance for clinical trials that use Decentralised Manufactured Investigational Medicinal Products (IMPs).
Guidance on transitional arrangements for the Clinical Trials Regulations.
Guidance on labelling for medicinal products used in clinical trials.
This guide gives an overview of the inspection data summary report (IDSR) for initial teacher education (ITE) providers and inspectors.
Submit information about your current caseloads if you're an intervention provider (IP) working on Prevent programmes.
Case study from Armilla.
These tools and techniques for civil servants across government provide guidance on implementing policy.
Introducing the new pre-application service for Nationally Significant Infrastructure Projects.
Armilla Verified is Armilla’s third-party verification of AI-powered products. It empowers AI vendors and enterprises alike to assure the quality and reliability of their AI solutions.
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