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Register to vote Register by 18 June to vote in the General Election on 4 July.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to use a cost utility analysis to evaluate your digital health product.
The Accelerated Access Review aims to speed up access to innovative drugs, devices and diagnostics for NHS patients.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
Aival Evaluate reports the performance, fairness, robustness and explainability of AI products under consideration on a user’s data, enabling comparison along the same baseline.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Use form ALVS1 if the Automatic Licence Verification System cannot process an automatic release on CHIEF or the Customs Declaration Service.
How to tax a beneficial loan arrangement for a director or employee.
Apply for an Individual Vehicle Approval (IVA) test for cars, goods vehicles, buses and coaches, and trailers on the technical application submission (TAS) service
How to apply to the Upper Tribunal Immigration and Asylum Chamber (UTIAC), how much it can cost and what you can do if your application fails.
Type approval, individual (IVA), motorcycle single vehicle approval, voluntary approval, certificate of initial fitness, accessibility approval, fees, forms, replacement certificates
Form N294: Claimant's application for a variation order.
Find out about abusive and defeated tax arrangements, and how the legislation is applied.
Upper Tribunal Tax and Chancery decision of Judge Greg Sinfield and Judge Guy Brannan on 23 April 2024
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (11 March 2024) approved the medicine quizartinib (Vanflyta) to be used alongside chemotherapy as first line treatment for adults who have acute myeloid leukaemia (AML).
Check the availability and any issues affecting the Advance Valuation Ruling service.
Apply for a share valuation check for an award of shares under an employee shareholder agreement.
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