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News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How to write up and share your findings
How to use a quasi-experimental study to evaluate your digital health product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to use a contextual inquiry when developing your digital health product.
Share your reference data for use in projects and services outside your organisation.
How to use an interrupted time series to evaluate your digital health product.
Planning user research activities for each development phase helps you design a service that meets the needs of your users.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to define your participant criteria, find participants for research and handle incentives.
Helping public health practitioners conducting evaluations – choosing evaluation methods.
Guide for VCSE organisations on how to bid and win contracts with government
How to prepare and analyse the data you collected for your evaluation.
How to run research sessions with vulnerable participants.
A guide to documenting how you’ve collected your packaging data, known as your ‘methodology’. Online marketplaces affected by extended producer responsibility (EPR) for packaging must submit a methodology.
How to make a detailed record of what happens during a user research session.
What detailed information you need to send to HMRC to support your Research and Development (R&D) tax relief claim, and when and how to submit it.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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