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Data, Freedom of Information releases and corporate reports
The roadmap sets out the measures government is taking to maximise the future success of Freeports.
Information on the reasons behind human infectious disease emergence, including a timeline and a global map.
How to use an interrupted time series to evaluate your digital health product.
Comply with good pharmacovigilance practice and prepare for an inspection.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Using metadata to make it easier to catalogue, validate, reuse and share your data.
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
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