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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance on maintaining the quality of qualitative evaluation for use in Government research
How to use a cost utility analysis to evaluate your digital health product.
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)
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to set what you’ll evaluate digital outcomes, digital specialists, user research participants and studio suppliers on.
How to use an ethnographic study to evaluate your digital health product.
DFID rapid evidence assessments provide rigorous and policy relevant syntheses of evidence, carried out in 3-6 months.
Guidance on choosing evaluation study types and methods.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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
Information on group pre-challenge reviews, including what they are and when they can be requested.
How to use an interrupted time series to evaluate your digital health product.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
This guidance explains our competition process and how your proposal is assessed.
Employment Appeal Tribunal Judgment of Sarah Crowther, Deputy Judge of the High Court on 24 May 2024.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
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