France Reveals The Drugs That Are Most Likely To Require Post-Market RWE Studies

A study from the health technology assessment department of France’s national health agency, HAS, has identified which pharmaceutical products are most likely to receive a request for post-market studies. The agency hopes this information will aid in companies’ forward planning.

Real-World Data
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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...

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