All Biosimilars articles

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    Journal

    Unique aspects of biologic reference standards

    2025-01-10T08:50:00Z

    Reference standards are pivotal in ensuring pharmaceutical quality, especially for complex biologics. This article reviews definitions and classifications of reference standards as outlined by the US Food and Drug Administration (FDA), the World Health Organization (WHO) and the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Q6B and Q7 guidelines. It addresses types of standards based on source and use, with particular emphasis on the distinct requirements for biologics.

  • GENDEVS
    Journal

    Considerations for generics developers moving into the field of biosimilars

    2025-01-10T08:49:00Z

    Many generic developers have experience in both manufacturing and gaining US and EU approval for generics which are small molecule alternatives to the authorised original products. These developers possess the relevant skillsets to allow them to pursue the development of biosimilars, which are large molecule biologics highly similar to the authorised original products.

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  • RR-Jan-2025- half cover
    Contents

    January 2025 – Contents

    January 2025  |  Vol. 22  |  No. 1

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    Journal

    Regulatory complexities and challenges of biosimilars

    2022-06-15T10:09:00Z

    This continuing professional development (CPD) supplement focuses on the regulatory complexities and challenges associated with biosimilar products and their development. Although biosimilar products have been registered and approved for use in the EU for more than a decade, there is increasing speculation and excitement on the potential for biosimilars with increasingly complex structures, eg, multi-subunit, extensively post-translationally modified, and lipid-containing products.

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    Journal

    CMC considerations for US biosimilars development

    2022-04-18T15:18:00Z

    The US Biologics Price Competition and Innovation Act of 2009 (BPCI Act) provides an abbreviated licensure pathway for biosimilar products. This pathway brought the hope of lower cost biologics, perhaps similar to what was accomplished by generics for small molecule drugs. Twelve years have now passed since the BPCI Act and experience continues to be gained with biosimilars development… 

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    Journal

    Brexit: The regulatory landscape one year on

    2022-03-21T09:37:00Z

    A year since the UK departed from the EU, what has changed? The UK has started to depart from the EU in a number of different ways. This article will explore what has changed, how it came about and what to look out for as the relationship between the UK and EU, as well as the rest of the world, continues to evolve.