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Biosimilars - Regulatory, Clinical, and Biopharmaceutical Development (Hardcover, 1st ed. 2018)
Loot Price: R4,864
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Biosimilars - Regulatory, Clinical, and Biopharmaceutical Development (Hardcover, 1st ed. 2018)
Series: AAPS Advances in the Pharmaceutical Sciences Series, 34
Expected to ship within 12 - 17 working days
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This book provides a comprehensive overview of the biosimilar
regulatory framework, the development process and clinical aspects
for development of biosimilars. The development path of a
biosimilar is just as unique as a development path of a new drug,
tailored by the mechanism of action, the quality of the molecule,
published information on the reference product, the current
competitive environment, the target market and regulatory guidance,
and most importantly, the emerging totality of evidence for the
proposed biosimilar during development. For the ease of readers,
the book comprises of six sections as follows: Section I: Business,
Health Economics and Intellectual Property Landscape for
Biosimilars Section II: Regulatory Aspects of Development and
Approval for Biosimilars Section III: Biopharmaceutical Development
and Manufacturing of Biosimilars Section IV: Analytical Similarity
Considerations for Biosimilars Section V: Clinical aspects of
Biosimilar Development Section VI: Biosimilars- Global Development
and Clinical Experience Chapters have been written by one or more
experts from academia, industry or regulatory agencies who have
been involved with one or more aspects of biosimilar product
development. The authors and editors have an expertise in
commercialization and pricing of biosimilars, intellectual property
considerations for biosimilars, chemistry manufacturing controls
(CMC) and analytical development for biosimilars, regulatory and
clinical aspects of biosimilar development. Besides the industry
practitioners, the book includes several contributions from
regulators across the globe.
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