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First multiple sclerosis biosimilar approved in Europe

European Pharmaceutical Review

The European Commission (EC) has granted Sandoz the first marketing authorisation of biosimilar Tyruko ®* (natalizumab). Sandoz entered into a global commercialization agreement for biosimilar natalizumab with Polpharma Biologics in 2019. Sandoz has the rights to commercialise and distribute it in all markets under the deal.

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Educating Patients about Generic Drugs: Strategies for Success

Drug Patent Watch

They’re designed to be bioequivalent, meaning they have the same dosage, strength, route of administration, quality, and intended use as the original brand-name drug. “2021 Generic Drug & Biosimilars Access & Savings in the U.S. Food and Drug Administration. “Generic Drugs: Questions & Answers.”

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17th edition of CPHI & PMEC India inaugurated at India Expo Centre, Noida

Express Pharma

Spanning pharma machinery, packaging, analytical instruments, laboratory technologies, ingredients, and beyond, it offers a comprehensive platform for stakeholders to engage in transformative dialogues and foster strategic partnerships. With exports nearing $27.84

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