Tag: MHRA
UK Medical Device Manufacturers Must Navigate New MHRA Registration System Post-Brexit
Medical device manufacturers must now register separately with the UK's MHRA for market access in Great Britain and Northern Ireland…
UK’s MHRA Launches Innovation Guidance to Accelerate Medical Device and Drug Development
The UK's MHRA has published formal guidance for drug and medical device developers, offering free access to regulatory expertise to…
MHRA publishes register of authorised online medicine sellers in Northern Ireland
The MHRA has published a searchable register of all websites authorised to sell medicines online in Northern Ireland, enabling patients…
UK’s MHRA Publishes Performance Data: Drug Approvals, Review Times, and Regulatory Efficiency Metrics
The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has published comprehensive performance data on drug approvals, review timelines, and…
UK Regulators Issue Five Medical Device Safety Alerts in Mid-June 2026
The UK Medicines and Healthcare products Regulatory Agency (MHRA) issued five field safety notices between 15 and 19 June 2026,…
UK Orphan Drug Registry Expands Access to Rare Disease Treatments
The UK Medicines and Healthcare products Regulatory Agency (MHRA) maintains a comprehensive registry of authorised orphan medicinal products for rare…
UK Regulators Issue Warning on Unlicensed Weight-Loss Drugs and False Marketing Claims
UK regulators have issued a joint warning against businesses promoting unlicensed weight-loss medicines and newly authorised prescription drugs with false…
UK and US Regulators Launch Joint Liaison Programme to Strengthen Drug Approval Coordination
The UK Medicines and Healthcare products Regulatory Agency (MHRA) and US Food and Drug Administration (FDA) have launched a formal…