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Global Health · page 4

UK, EU & international health agencies

MHRA (UK) · Jul 29, 2026

Guidance: Ambient voice technology-enabled products

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.

MHRA (UK) · Jul 27, 2026

Safety Public Assessment Reports

These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.

EMA (EU) · Jul 24, 2026

Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 20-23 July 2026

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…

MHRA (UK) · Jul 24, 2026

No summer shortcut for safe weight loss

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.

UKHSA (UK) · Jul 23, 2026

Accredited official statistics: Monthly mandatory surveillance of MRSA, MSSA, Gram-negative bacteraemia and C. difficile infections, June 2025 to June 2026

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.

MHRA (UK) · Jul 23, 2026

Clinical investigations in Great Britain

How manufacturers should undertake a clinical investigation for a medical device to ensure they comply with medical device regulations.

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