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Data, Freedom of Information releases and corporate reports
How to use an interrupted time series to evaluate your digital health product.
Guidance for exporting nuclear equipment, material and technology that appears on what is known as the 'Trigger List'.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Animal bites and pasteurella infections information for healthcare staff.
Employment Appeal Tribunal Judgment of Mrs Justice Eady, Mrs Gemma Todd, and Dr Gillian Smith on 15 July 2024.
Get help to classify textiles and which headings and codes to use.
Get help to classify various types of vehicles such as mobility scooters, dumpers and utility vehicles, all-terrain vehicles and e-bikes for import and export.
How to use a quasi-experimental study to evaluate your digital health product.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Check what security features you’ll need put on tobacco product packaging.
Understand the definition of ‘director’ so you know if you need to apply for a licence.
The role of the Grants Management Function, the Centre of Excellence service offer, and the Functional Standard for Grants.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to use an N-of-1 study to evaluate your digital health product.
How to use a cost benefit analysis to evaluate your digital health product.
Find out about the long-term effects some people can have after having COVID-19.
How to use a factorial randomised controlled trial to evaluate your digital health product.
How to use a cost utility analysis to evaluate your digital health product.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
The symptoms and diagnosis of Orf.
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