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Register to vote Register by 18 June to vote in the General Election on 4 July.
How to use a crossover randomised controlled trial 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.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
Information to help you identify if your organisation needs to publish a modern slavery statement.
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.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to use a cost benefit analysis to evaluate your digital health product.
How to use a quasi-experimental study to evaluate your digital health product.
How to set out your charity's purposes and rules in its governing document, how to start using it and how to change it.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Tell HMRC about premises you want to include in, or remove from your entry on the Gaming Duty Register using form GD58.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Get help to classify cigarettes, cigars, raw tobacco, smoking tobacco, tobacco for heating and nicotine substitutes for import and export.
Find helpsheets, forms and notes to help you fill in the capital gains pages of your Self Assessment tax return.
Information and guidance for local authorities compiling the P1E quarterly data returns on homelessness.
Find out what areas the Scottish administration legislates on and how it is structured.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
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