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Latest From Polpharma SA

EMA Says Yes To Janssen’s Talvey & 13 Other Drugs

Fourteen new products could be approved in the EU soon, after the European Medicines Agency gave them the thumbs up.

Europe Approvals

Triple Threat: EMA Endorses Three First-Time Biosimilars

At an eventful European Medicines Agency committee meeting in July, three biosimilars from Biocon, Sandoz and Fresenius Kabi have become the first for each respective molecule – aflibercept, natalizumab and tocilizumab – to gain the endorsement of the CHMP.

Biosimilars Regulation

EU Crunch Time For Previously Rejected Lagevrio & Other New Drugs

MSD/Ridgeback Biotherapeutics’ COVID-19 treatment Lagevrio is among the products that are up for an opinion this week from the European Medicines Agency on whether they should be recommended for use across the EU.

Europe Approvals

Generics And Biosimilars Industry Reshaped By Transformations

The latest Generics Bulletin Top 50 ranking of global generics and biosimilars companies sees a new name in the top five amid transformations for some of the leading off-patent players. Meanwhile, a number of mid-level firms shift position and newcomers climb into the bottom of the table.

Outlook 2023 Generic Drugs
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