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Register to vote Register by 18 June to vote in the General Election on 4 July.
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.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Following MHRA approval of a clinical trial, early breast cancer patients on endocrine-based therapy can benefit from a study with camizestrant.
The characteristics, diagnosis, treatment, and epidemiology of group B streptococci.
Read about talking therapies and counselling for mental health problems.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Find out about partial exemption and the methods and calculations to use to see how much input tax you can recover.
How to meet the general binding rules if your septic tank or small sewage discharge treatment plant releases (discharges) waste water to a surface water.
First-of-its-kind counselling and 24/7 support for jurors following difficult cases.
An open-label, non-inferiority, randomised controlled trial
Visit the UK as a Standard Visitor for tourism, business, study (courses up to 6 months), medical treatment and other activities. Find out whether you need a Standard Visitor visa, or can visit without a visa.
How to get a marketing authorisation for an Advanced Therapy Medicinal Product (ATMP) so it can be sold and/or supplied in Great Britain.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
We’re responsible for handling appeals against decisions by the Secretary of State for Education, the Secretary of State for Health, Care Quality Commission, Ofsted or the Care Council of Wales which exclude, remove or suspend you from a register to...
Standardisation explained.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
The pre-clinical evaluation team at VDEC provides a safe and controlled environment to test new vaccines and therapeutics before they progress to clinical trials
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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