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A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
VDEC works with global leaders from all sectors to develop and deliver the vaccine and therapeutic products we need to protect us from infectious diseases.
This guidance relates to Technical Standards and Standard Development Organisations to describe the typical first step in a Standard Essential Patent (SEP) journey.
How to apply for a full or partial completion certificate after building work on a higher-risk building has been completed.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
How to use a quasi-experimental study to evaluate your digital health product.
Using an ecological momentary assessment to evaluate your digital health product.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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