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6 December 2022 | By Cécile Matthews (CRA), Charlotte Capdevila
When France's ATU reform was implemented, some viewed it as restrictive. Here, Cécile Matthews and Charlotte Capdevila explore the reform’s impact on early access to oncology drugs and products for rare diseases.
6 December 2022 | By Catherine Eckford (European Pharmaceutical Review)
The top 20 biopharma companies averaged a market capitalisation decline of $3.45 trillion in Q2 to $3.14 trillion in Q3 2022, says GlobalData.
14 December 2020 | By Victoria Rees (European Pharmaceutical Review)
The EMA's human medicines committee has released its results for the December meeting, suggesting which therapies should receive marketing authorisation.
30 August 2019 | By Victoria Rees (European Pharmaceutical Review)
This August saw nine new green lights from the FDA, all small molecules, which makes up a third of the approvals this year.
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