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Supporting guidance, publications and resources on the use of real-world data (RWD) and real-world evidence (RWE) in regulatory decision-making for medicines and medical devices in the UK.
Commissioning letter to the Science and Technology Ethics Advisory Committee setting out work priorities for 2026 to 2027.
Twenty-eight members of CoEHAR are featured in the 2026 World’s Top 2% Scientists database, bringing international recognition to the breadth and scientific impact of the research community behind the Center. […]
Find out how the Digital Mental Health Technology Working Group supported MHRA and NICE work on regulation, evaluation and AI priorities for DMHTs.
In the final instalment of our strategy blog series, MHRA Chair Professor Anthony Harnden reflects on the insights shared throughout the series and how innovation and collaboration across the UK are shaping the future of healthcare regulation.
Letters between the chair of the Social Security Advisory Committee (SSAC) and the DWP Minister for Lords.
Statistics on incidents where police officers use force; including type of force, reason, outcome, injuries, and person details (such as age, gender).
The Food and Drug Administration (FDA or the Agency) has determined the regulatory review period for MONOFERRIC and is publishing this notice of that determination as required by law. FDA has made the determination because of the submission of an application to the Director of...
The Food and Drug Administration (FDA) is classifying the hematopoietic cell enrichment kit into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the hem...
The Food and Drug Administration (FDA, the Agency, or we) is announcing a public meeting titled "Challenges and Solutions in Lot- Level Food Traceability." The purpose of the meeting is to provide a forum for the public to share information on continued implementation of the "...
Private renters are next to benefit from the protections of Awaab's Law. A government consultation is now open, looking at how to implement these new rights.
JTI said the factory had been struck several times and that operations were suspended before the latest attacks. The company said all employees were safe. The post Russia Attacks JTI Subsidiary in Ukraine first appeared on Tobacco Reporter.
He also requested communications between FDA officials and Altria, Reynolds American, their subsidiaries, and other parties involved in challenges to the rules. The post Ill. Rep Questions FDA Review of Vape Rules first appeared on Tobacco Reporter.
The measure will run through 2032, with regions able to adopt their own laws imposing the bans. The post Russia to Allow Regional Vape Sales Bans first appeared on Tobacco Reporter.
The FDA received more than 26.6 million applications from 2018 through 2025 and completed reviews of about 26.5 million. The post GAO Finds FDA Holding 130K Tobacco Applications to End 2025 first appeared on Tobacco Reporter.
