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A white paper: US biosimilars market on pace with Europe

Published in: Volume 9 / Year 2020 / Issue 4
Page: 150-4
Author(s): Madelaine A Feldman, MD, FACR, Michael S Reilly, Esq

Abstract: In the US, 28 biosimilars have been approved, with 10 in the last two years. The US is keeping pace with the EU who pioneered biosimilars approvals a decade… Read More »

European prescribers’ attitudes and beliefs on biologicals prescribing and automatic substitution

Published in: Volume 9 / Year 2020 / Issue 3
Page: 116-24
Author(s): Madelaine A Feldman, MD, FACR, Michael S Reilly, Esq

Introduction: The European Union (EU) and the European Medicines Agency (EMA) have led the development of a regulatory framework for biosimilars since 2004. By end of December 2019, 64 biosimilars… Read More »

Clear naming, traceability of biological medicines will protect patients

Published in: Volume 6 / Year 2017 / Issue 4
Page: 153-4
Author(s): Alejandro Mercedes, MD, Associate Professor Valderilio Feijó Azevedo, MD, PhD, MSc, Brian Bressler, MD, Madelaine A Feldman, MD, FACR

Author byline as per print journal: Adjunct Professor Valderilio Feijó Azevedo, MD, PhD, MBA; Associate Professor Brian Bressler, MD, MS, FRCPC; Madelaine A Feldman, MD, FACR; Professor Alejandro Mercedes, MD Abstract:… Read More »