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Register to vote Register by 18 June to vote in the General Election on 4 July.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
Compare different evaluation approaches and choose an appropriate method.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidance on choosing evaluation study types and methods.
How consumers can reduce their energy costs by getting a group deal
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Find out the information you must give to customers on food products and how to give it.
Ensuring you get what you pay for.
How to use a cost effectiveness analysis 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.
How to use an economic evaluation to evaluate your digital health product.
Use these general provisions to help you determine the origin of your products.
How to create a model of how your digital health product works and choose measures for your evaluation.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How to use a randomised controlled trial to evaluate your digital health product.
Things to consider when buying and using products.
How to use a case-control study to evaluate your digital health product.
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