What lurks in the shadows of the openness hyperbole for biopharmaceuticals?

Neethu Rajam, Timo Minssen

    1 Citation (Scopus)

    Abstract

    Recent advances in transparency initiative signify laudable developments. Yet, a closer look on the legal developments indicates that commercially confidential information and personal data will continue to pose persisting challenges for clinical trial transparency and drug development. This article depicts these developments with a particular focus on European Medicines Agency (EMA) and Biologics. We argue that in order to promote the development of innovative biologics and biosimilars, the EMA will need to carefully consider and address such challenges.

    Original languageEnglish
    JournalDrug Development Research
    Volume80
    Issue number3
    Pages (from-to)282-284
    Number of pages3
    ISSN0272-4391
    DOIs
    Publication statusPublished - 11 May 2019

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