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Safety Evaluation of Biotechnologically-derived Pharmaceuticals - Facilitating a Scientific Approach (Hardcover, 1998 ed.)
Loot Price: R3,141
Discovery Miles 31 410
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Safety Evaluation of Biotechnologically-derived Pharmaceuticals - Facilitating a Scientific Approach (Hardcover, 1998 ed.)
Series: Centre for Medicines Research Workshop
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Considerable investment has been made by both pharmaceutical and
biotechnology companies in pharmaceutical products of
biotechnology. However, because relatively few of these products
have been marketed, lack of relevant experience means that
uncertainty still surrounds the most appropriate strategy for their
safety evaluation. The 13th CMR International Workshop, held in
February 1997, provided the opportunity for regulatory authority
and industry experts from Europe, Japan and the USA to share their
experiences of designing safety evaluation programmes for specific
product classes: colony stimulating factors, growth factors,
hormones, interferons, interleukins, monoclonal antibodies for
therapeutic use, and gene therapy products. Participants worked
together to recommend those studies that should be considered for
such safety evaluation, and those that may be unnecessary. These
recommendations subsequently made a valuable contribution to the
ICH guideline Safety Studies for Biotechnological Products', which
was finalised at ICH 4 in Brussels in July 1997. The Workshop
proceedings not only describe the recommendations but also provide
the reader with an appreciation of the science behind safety
evaluation strategies used by experts, the influence of different
regulatory systems on these strategies, and the type of data
required by both toxicologists and clinicians before they have
sufficient confidence to administer pharmaceutical products of
biotechnology to humans.
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