"Nonclinical Development of Novel Biologics, Biosimilars,
Vaccines and Specialty Biologics" is a complete reference devoted
to the nonclinical safety assessment of novel biopharmaceuticals,
biosimilars, vaccines, cell and gene therapies and blood products.
This book compares and contrasts these types of biologics with one
another and with small molecule drugs, while incorporating the most
current and essential international regulatory documents. Each
section discusses a different type of biologic, as well as early
characterization strategies, principles of study design,
preclinical pharmacokinetics and pharmacodynamics and preclinical
assays. An edited book that is authored by leading experts in the
field, this comprehensive reference provides critical insights to
all researchers involved in early through late stage
biologics.
Provides in-depth coverage of the process of nonclinical safety
assessment and comprehensive reviews of each type of
biopharmaceuticalContains the most pertinent international
regulatory guidance documents for nonclinical evaluationCovers
early de-risking strategies and designs of safety assessment
programs for novel biopharmaceuticals and vaccines, as well as
follow-on biologics or "biosimilars"A multi-authored book with
chapters written by qualified experts in their respective
fields
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