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This document provides guidance on the data integrity expectations that should be considered by organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA.
Rotavirus immunisation information for public health professionals.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Documents to help local authorities and providers commission and deliver maternal and child public health services from preconception up to 24 years.
Who can supply and or administer specific medicines to patients without a doctor under a PGD and which medicines can be administered.
This document sets the standards and lists the essential topics which should be incorporated into immunisation training for registered healthcare practitioners.
A leaflet to send to women referred for colposcopy, after an abnormal cervical screening result.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Guidance on security measures for transporting controlled drugs in the UK or internationally.
This leaflet explains the measles mumps rubella (MMR) vaccine for all ages.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
Guidance for health clearance of healthcare workers (HCWs) and management of those infected with bloodborne viruses (BBVs) hepatitis B, hepatitis C and HIV.
Toolkit and resources for local authorities and other stakeholders to raise awareness of the potential risks created by ticks and tick-borne disease in England.
Information for healthcare professionals on pertussis (whooping cough).
Advice to give pregnant women on infections that can be transmitted via contact with animals that are or have recently given birth.
Information leaflet and sticker for the COVID-19 autumn vaccination programme.
Medicines and Healthcare product Regulatory Agency official Parental Leave policy and procedures.
Information and promotional resources to support the 2024 to 2025 annual flu vaccination programme.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Guidance on licencing and best use of radiopharmaceuticals and sealed radioactive sources in diagnosis, treatment or research.
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