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Guidance on labelling for medicinal products used in clinical trials.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Guidance for manufacturers of cardiac implantable electronic devices and their leads. It outlines specific scenarios that should be considered when determining if an incident is reportable.
Guidance on using non-investigational medicinal products in a clinical trial.
Check what side effects people have reported when they have taken a medicine.
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
Find out details of the procedure codes and additional procedure codes that are excluded from use with Simplified Declaration Procedure (SDP) with regular use and Entry in Declarants Records (EIDR).
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
International trade mark registrations protected in the EU under the Madrid Protocol will no longer enjoy protection in the UK after 1 January 2021.
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