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An overview of risks to pregnant women from infections: current screening, vaccination, treatment and prevention programmes.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Urgent safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Q fever (Coxiella burnetii) causes illness and sometimes abortion in animals, and it can lead to a pneumonia-like illness in humans.
Following MHRA approval of a clinical trial, early breast cancer patients on endocrine-based therapy can benefit from a study with camizestrant.
Information on the programme, including the screening tests, commissioning, quality assurance, education and training.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Weekly national influenza and COVID-19 report, COVID-19 activity, seasonal flu and other seasonal respiratory illnesses.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Protocols and procedures for testing the value for cultivation or use (VCU) of agricultural crops.
Guidance on how Ofsted regulates childcare.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
We lead the government’s efforts to make the United Kingdom the best place to be a veteran anywhere in the world, helping the nation fulfil its lifelong duty to those who have served in the armed forces. OVA is part...
Statistics on primary school children who are overweight, measured in reception and year 6 and presented for different ethnic groups.
Information for early years providers, childminders and nurseries including guidance on the early years foundation stage (EYFS), funding and training.
This form provides assistance in identifying the key areas of compliance required in respect of primary care premises development.
Information on granted EAMS scientific opinions, including the public assessment report and treatment protocols.
An explanation of what happens to those judged inadequate on the Early Years Register and those not meeting registration requirements on the Childcare Register.
The MHRA has authorised cabotegravir as 30 mg tablets and as a 600 mg long-acting injection administered every two months
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