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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.
Work to develop the Government Chemist capabilities in food fraud through the identification and quantification of food adulterants.
This page collects research analysis documents from the Evaluation and Analysis teams at Building Digital UK (BDUK)
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
This series brings together all documents relating to Research
These publications provide analyses and data that are not classified as research or official statistics.
This collection brings together all documents in the Employment Relations Research Series.
How to use a randomised controlled trial to evaluate your digital health product.
View highlights of some of our most recently published research on this page. You can also download a complete list of our published research.
Compare different evaluation approaches and choose an appropriate method.
This collection brings together all documents relating to DWP communications and customer insight research.
The government responds to a report by the Advisory Council on the Misuse of Drugs and commissions Part 2 of work on barriers to research.
The MHRA is ready to provide any assistance for clinical trials applications submitted for COVID-19
Submission dates and how the submissions using the EC decision reliance procedure work.
There are different model agreements for management of Intellectual Property (IP) in collaborative research in the UK and overseas.
How to use a feasibility study when planning the evaluation of your digital health product.
We are producing guidance and information for industry, healthcare professionals and patients covering the coronavirus (COVID-19) outbreak.
How to use a behaviour change techniques review to evaluate your digital health product.
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