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Register to vote Register by 18 June to vote in the General Election on 4 July.
Upper Tribunal Administrative Appeals Chamber decision by Judge Stout on 2 May 2024.
Find out if you need to apply for the fit and proper test and how to do this so that HMRC can register your business.
Guidance primarily aimed at local responders covering some humanitarian issues that may arise during the recovery phase of an emergency in the UK.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to use a randomised controlled trial to evaluate your digital health product.
Employment Appeal Tribunal Judgment of Mr Justice Kerr on 23 May 2024.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
Compliance Audit applies to organisations receiving funding under Homes England affordable housing programmes.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Licensing bodies and collective management organisations can agree licences with users on behalf of owners and collect any royalties the owners are owed.
Guidance on the collection and reporting of data for CTAD, the surveillance system for all chlamydia tests done in England.
Grievances and disciplinary action at work can be solved by informal discussions, formal procedures, mediation, conciliation or arbitration.
Advice to British people affected by crises abroad such as large-scale terrorist attacks, natural disasters and political unrest, and how the FCDO can help.
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.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to use a quasi-experimental study to evaluate your digital health product.
We’re working to help people securely prove who they are without having to rely on physical documents.
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.
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