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Register to vote Register by 18 June to vote in the General Election on 4 July.
Design, build and operate APIs in a consistent way
Information to help school leaders plan, develop and implement the new statutory curriculum.
How a competent authority must decide if a plan or project proposal that affects a European site can go ahead.
Guidance to support education settings who want to use external expertise to enhance their online safety education.
Submissions related to human medicines need to be submitted directly to the MHRA.
The Regulatory Policy Committee provides the government with external, independent scrutiny of the evidence supporting changes in law that affect businesses, charities and community groups.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Upper Tribunal Administrative Appeals Chamber decision by Judge Brunner on 3 May 2024.
How to arrange an effective external review of governance and improve the performance of your board.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
What best available techniques are, when you must follow them, how to propose alternatives and how to refer to them in your application.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Share your reference data for use in projects and services outside your organisation.
BAT for diesel engines on an installation that are classed as new medium combustion plant, operating up to 500 hours a year that are exempt from emission limit values (ELVs).
This guidance is designed to help UKHSA customers and partners to navigate engaging and working with us and to signpost upcoming events and opportunities.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Advises on how to consider light within the planning system.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Helping public health practitioners conducting evaluations on how to plan them.
Find out the information you must give to customers on food products and how to give it.
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