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Data, Freedom of Information releases and corporate reports
How to use a contextual inquiry when developing your digital health product.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use an interrupted time series to evaluate your digital health product.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Actions that trial sponsors should consider to build resilience into clinical trial design
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Find out if you can declare personal goods orally or by conduct.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to move and declare goods that have been imported or exported between the UK and the UK Continental Shelf.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
How to use a crossover randomised controlled trial to evaluate your digital health product.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
This series brings together all documents relating to ministerial conduct and guidance
This guidance is for Ofsted inspectors carrying out inspections of providers that are only registered on either or both parts of the Childcare Register.
How investigators and sponsors should manage clinical trials during COVID-19
How to use a quasi-experimental study to evaluate your digital health product.
Comply with good pharmacovigilance practice and prepare for an inspection.
Helping public health practitioners conducting evaluations – identifying when it is possible and appropriate to evaluate.
Planning the practicalities and managing or conducting your evaluation.
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