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28 February 2022 | By European Pharmaceutical Review
Highlights of the February 2022 meeting of EMA’s human medicines committee (CHMP) include the recommendation of 13 medicines for approval, along with updates to other drugs and COVID-19 vaccines.
17 November 2021 | By Anna Begley (European Pharmaceutical Review)
The European Commission (EC) has granted marketing authorisation for Vumerity® to treat adults with relapsing-remitting multiple sclerosis.
31 October 2019 | By Victoria Rees (European Pharmaceutical Review)
VUMERITY has been granted approved by the FDA for the treatment of relapsing forms of multiple sclerosis based on data from a New Drug Application submission.
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