Medicines that either have a questionable level of added benefit or are innovative products for which a substantial benefit is expected but where evidence uncertainties remain are the most likely to be met with requests for post-market data collection, according to a new study from the health technology assessment (HTA) department at France’s HAS (Haute Autorité de Santé).
The study was conducted with the intention of helping pharmaceutical companies to better plan their strategies for collecting real-world evidence...








