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.

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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).

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