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Register to vote Register by 18 June to vote in the General Election on 4 July.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Environmental regulations and guidance on offshore oil and gas exploration and production, offshore gas unloading and storage and offshore carbon dioxide storage activities
How to join the phase I accreditation scheme.
Check when packaging is classified as a finished plastic packaging component, and what is meant by substantial modifications, to find out if you must register for the tax.
Guidance for anyone in the public sector that wants to apply for GovTech Catalyst funding to help solve a problem.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Find out more about what you need to do as a challenge owner.
How to apply for a completion or partial completion certificate after contractors have completed the building work for higher-risk building work or building work to an existing higher-risk building.
Guidance on the examination stage for Nationally Significant Infrastructure Projects.
How to use a multiphase optimisation strategy (MOST) to evaluate your digital health product.
This guide provides an overview of the inspection data summary report (IDSR) for primary and secondary schools, including schools with a sixth form and gives guidance on interpreting the data.
The Building Safety Fund (BSF) provides funding to fix life safety fire risks associated with cladding in buildings over 18 metres high. This guide explains the process.
How investigators and sponsors should manage clinical trials during COVID-19
A table of rehabilitation periods for the most common sentences and disposals, and example scenarios.
Guidance primarily aimed at local responders covering some common issues that may arise during the Recovery Phase of an emergency in the UK.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
What to do in discovery, how long it takes, how you know it's finished and deciding when to move on.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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