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The characteristics, diagnosis, management, and epidemiology of group C streptococci and group G streptococci.
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Department of Health and Social Care and MHRA register of licensed wholesale distribution sites (human).
Guidance on labelling for medicinal products used in clinical trials.
Information on clinical trials for medicines, how to apply for authorisation in the UK, how to manage your authorisation, reporting safety issues and details about the MHRA phase I accreditation scheme.
This collection brings together information on the UK’s international obligations in the field of human rights.
The MHRA register of licensed manufacturing sites: manufacturer specials - human (MS) and manufacturer specials authorisation - veterinary (MANSA) only.
Information on the diagnosis, prevention and treatment of human parainfluenza viruses (HPIVs).
Statement following the meeting of the G7+ Special Representatives for Afghanistan on 29-30 September 2025
Guidance on using non-investigational medicinal products in a clinical trial.
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