Alerts

Regulators Start Writing the Rules for AI-Driven Medicines
The joint FDA-EMA principles for AI in drug development show regulators trying to align before AI becomes embedded across discovery, trials, manufacturing and post-market safety.

England’s Tirzepatide Rollout Shows Approval Is Not Access

Medicare’s GLP-1 Bridge Turns Obesity Coverage Into a Public-Payer Experiment

WHO Makes Obesity Treatment a Global Access Test

Alzheimer’s Agitation Gets a New Drug, But Care Pathways Still Lag

Huntington Gene Therapy Hits the Evidence Wall

Rare Disease Policy Moves Into the Individualised Therapy Era

Alzheimer’s Access Now Starts With Genotyping and MRI Capacity

AI Mental Health Support Becomes a Governance Test

Alzheimer’s Drugs Force NICE Back Into the Value Debate
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