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Find out about coronavirus (COVID-19) treatments available outside of hospital, including information on free prescriptions and lateral flow tests.
Read about talking therapies and counselling for mental health problems.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use a randomised controlled trial to evaluate your digital health product.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to use a cost effectiveness analysis to evaluate your digital health product.
How to process manure, guano or digestive tract content for sale as a fertiliser in the EU, including how to propose a new treatment method.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
What best available techniques are, when you must follow them, how to propose alternatives and how to refer to them in your application.
Guidance on the pre-application stage for Nationally Significant Infrastructure Projects.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
How UK citizens or residents can get healthcare when visiting countries or territories outside the EU where the UK has reciprocal healthcare agreements.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How to apply for alternative dispute resolution and when you can use it to resolve a tax disagreement with HMRC.
How the MHRA makes decisions on what is a medicinal product (borderline products).
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
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