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Register to vote Register by 18 June to vote in the General Election on 4 July.
Find out how to link your temporary storage facility to Customs Handling of Import and Export Freight (CHIEF) or the Customs Declaration Service using a Community Systems Provider.
Guidance for manufacturers, importers and distributors.
Find out about military instructor training and personal development courses, provided by BMATT (CZ), to promote international co-operation.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
The Private Finance team is the main point of contact for current and potential lenders, investors, ratings agencies and advisors.
We work with experts to generate analysis and ideas for policy.
Find out how to import your personal belongings, pets and private motor vehicles when moving or returning to the UK.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Find out what the MOD War Detectives get up to throughout their days
When military end-use export controls apply and to which destinations.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to use a case-control study to evaluate your digital health product.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
Skills a service team needs to deliver a successful user-focused service.
The VDEC clinical evaluation team works to support vaccine and therapeutic development by providing expertise in immunological and functional assays used to support clinical trials (Phase I to IV)
Submissions related to human medicines need to be submitted directly to the MHRA.
Follow this guidance when you want to get spend approval for commercial activities costing £20 million or more excluding VAT.
How to use a crossover randomised controlled trial to evaluate your digital health product.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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