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Departments, agencies and public bodies
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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to create a model of how your digital health product works and choose measures for your evaluation.
What you need to know about and do to comply with the law and keep consumers safe.
How to use a micro-randomised trial to evaluate your digital health product.
How to write up and share your findings
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
Things to consider when buying and using products.
How to use feedback from marketplace reviews to evaluate your digital health product.
Why it's important to evaluate digital health products that have been developed rapidly and how to choose evaluation methods in these circumstances.
Information on OPSS product safety alerts, reports and recalls for unsafe products and resources for consumers, businesses and regulators.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Tax and reporting rules for employers providing awards for employee suggestions
How to use a cost benefit analysis to evaluate your digital health product.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to use focus groups to evaluate your digital health product.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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