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Sets out process and expectations on pre-application discussions.
Supports effective delivery of planning application process.
Fees guidance: explains planning related fees and the method of calculating them.
Use this form and guidance to apply for a capital grant for an Implementation Plan (PA1) or Feasibility Study (PA2).
Learn how the Government Digital Service is monitoring accessibility under the Public Sector Bodies (Websites and Mobile Applications) (No.2) Accessibility Regulations 2018.
Use this form and guidance to apply for a capital grant for an implementation plan (PA1) or feasibility study (PA2).
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
How to apply for a letter of approval from the Environment Agency to participate in CDM and JI projects.
Make an urgent or emergency application to get permission to make decisions for someone who lacks mental capacity including interim applications for people applying to be a deputy
Use this guidance and forms to apply for funding to support the production of a UK Forestry Standard compliant woodland creation plan.
This form covers applications for data held by Ministry of Justice, the MOJ DfE share and data held by HM Courts & Tribunals.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
This code of practice sets out minimum security and privacy requirements for app store operators and app developers.
Use this form to apply to register one or more designs.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This form is to be completed by a member of a public authority seeking authorisation to use covert human intelligence sources (CHIS).
Documents that provide advice and information on submitting applications to the Advisory Committee on Borderline Substances (ACBS).
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Don’t include personal or financial information like your National Insurance number or credit card details.
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