France's health technology assessment authority, whose Transparency Committee rates the added clinical benefit of each new cancer drug and so sets its price and reimbursement.
Created in 2004, the HAS is an independent public authority that evaluates medicines, devices and procedures for reimbursement and produces clinical guidelines. Its Commission de la Transparence assigns each drug a clinical benefit score (SMR) and an improvement in clinical benefit rating (ASMR I-V) that drive price negotiations with the Comité Économique des Produits de Santé; France's early access programme (accès précoce, formerly ATU) lets patients receive promising cancer drugs before marketing authorisation, with HAS deciding eligibility. HAS also accredits hospitals, runs the screening programme guidance and participates in the EU joint clinical assessments beginning with oncology in 2025.
Director General of the Haute Autorité de Santé, responsible for the agency's operations since January 2024.
Physician and former university president who chairs the Haute Autorité de Santé, France's health technology assessment and quality body.
Shares Gemeinsamer Bundesausschuss / IQWiG, National Institute for Health and Care Excellence, Real-world evidence, Prices and value.
Shares ISPOR (The Professional Society for Health Economics and Outcomes Research), National Institute for Health and Care Excellence, Real-world evidence, Prices and value.
Shares Gemeinsamer Bundesausschuss / IQWiG, European Medicines Agency, National Institute for Health and Care Excellence, Prices and value.
Shares France: early access (accès précoce), formerly ATU, EU HTA Regulation (EU) 2021/2282: joint clinical assessments, Gemeinsamer Bundesausschuss / IQWiG, Prices and value.
Shares ISPOR (The Professional Society for Health Economics and Outcomes Research), National Institute for Health and Care Excellence, Real-world evidence, Prices and value.
Shares Institut Curie, Gustave Roussy, UNICANCER.
Shares Lionel Collet, France: early access (accès précoce), formerly ATU, EU HTA Regulation (EU) 2021/2282: joint clinical assessments, Real-world evidence.
Shares EU HTA Regulation (EU) 2021/2282: joint clinical assessments, European Medicines Agency, Prices and value, Most of the world has almost no cancer care.