Promotional material: Vaccine update: issue 373, July 2026
Latest developments in vaccines, vaccination policies and procedures for immunisation practitioners.
UK, EU & international health agencies
Latest developments in vaccines, vaccination policies and procedures for immunisation practitioners.
Device qualification and classification of ambient voice technology-enabled products that are medical devices intended to be placed on the market, or put into service, in Great Britain.
Helping manufacturers define the characteristics of their devices and determine the appropriate regulatory qualification and classification.
Information for healthcare professionals on the diagnosis and treatment of infant botulism, foodborne botulism and wound botulism.
Official statistics in development estimating the size and composition of the life sciences sector in the UK.
List of Field Safety Notices from 20 to 24 July 2026.
Identification and management of outbreaks and resources to support local health protection system response to outbreaks of communicable disease.
World Hepatitis Day is an opportunity to raise awareness of the risk of contracting hepatitis and the health threats it can bring, while at the same time recognising the progress Europe has made to strengthen prevention.
While Europe has made steady progress in preventing hepatitis B and C the region is set to miss the 2030 target to eliminate viral hepatitis as a public health threat.
Hundreds of thousands of women have accessed the morning-after pill at high street pharmacies in the first 5 months since the NHS made it available free-of-charge. New NHS figures show that almost 305,000 doses of the emergency contraceptive pill were supplied at pharmacies between October 2025 and March 2026 without women needing to book a […]
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Public Assessment Report on the safety review of the available data on the risk of dementia with the use of bladder anticholinergic medicines.
An amber heat-health alert has been issued for the East Midlands, East of England, South East and London.
Reports on departmental staff numbers and costs.
Guidance for health professionals delivering the time-limited MenB vaccination offer on the eligible cohort.
Information for academic authorities and students on pre-registration healthcare programmes in the 2026 to 2027 academic year.
Twelve new medicines recommended for approvalEMA’s human medicines committee (CHMP) recommended twelve medicines for approval at its July 2026 meeting.The committee…, CHMP statistics Key figures from the July 2026 CHMP meeting are represented in the graphic below. © European Medicines Agency , CHMP statistics:…, Positive recommendations on new medicines, Evlarco International non-proprietary name (INN) obicetrapib / ezetimibe Marketing authorisation applicant A. Menarini International Licensing S.A.…, Icotyde INN icotrokinra hydrochloride Marketing authorisation…
As demand for weight-loss medicines continues to rise, the MHRA is reminding people how to use GLP-1 medicines safely, spot illegal sellers, and avoid diet changes that could interfere with their medicines.
Mandatory surveillance of healthcare-associated infections (HCAI), which include methicillin-resistant Staphylococcus aureus (MRSA), Methicillin-sensitive Staphylococcus aureus (MSSA), Gram-negative bacteraemia such as Escherichia coli (E. coli), Klebsiella and Pseudomonas aeruginosa (P. aeruginosa) and Clostridioides difficile (C. difficile, or CDI): June 2025 to June 2026.
How to notify the MHRA that you are going to undertake a clinical investigation of a medical device.
How to determine if you will need to undertake a clinical investigation of a medical device, or if it is exempt under the regulations.
How manufacturers should undertake a clinical investigation for a medical device to ensure they comply with medical device regulations.
How the MHRA decides whether to approve a clinical investigation for medical devices.
Neuraxpharm UK Ltd has informed the MHRA of missing safety information in the Patient Information Leaflet (PIL) and Summary of Product Characteristics (SmPC) for certain batches of Tuzulby prolonged release 20mg, 30mg and 40mg chewable tablets.