Regulatory Practice for Biopharmaceutical Production -

Regulatory Practice for Biopharmaceutical Production

Buch | Hardcover
566 Seiten
1994
Wiley-Liss Inc.,U.S. (Verlag)
978-0-471-04900-5 (ISBN)
390,98 inkl. MwSt
Provides an overview of controversial regulatory issues in biotechnology, covering fundamental aspects, specific products and international perspectives. The licensing concerns critical to facility design and product manufacturing are discussed in detail.
Biotechnology represents a novel and expanding international industry bound by new and ever-changing legislature. This text provides a comprehensive overview of product-specific, international and country-specific licensing requirements and general regulatory issues in biotechnology.

Anthony S. Lubiniecki and Susan A. Vargo are the authors of Regulatory Practice for Biopharmaceutical Production, published by Wiley.

Partial table of contents:

A U.S.

View of New Biotechnology Regulation (H. Miller).

Genetic Stability of Host Cell and Product (M. Wiebe & N.Lin).

Quality Control Issues for the New Biotechnology (S. Vargo).

Strategic Decisions in Process Design (A. Lubiniecki).

Experience in Manufacturing, Testing, and Licensing a Hepatitis BVaccine Produced by Recombinant Technology (A. Elliott, etal.).

Tissue Plasminogen Activator: Regulatory Issues (D. Beebe & G.Murano).

Recombinant Peptide Hormones (Y.-y.

Chiu).

Cytokine and Growth Factor Products (L. Dujack & K.Zoon).

Licensing Biotechnology Facilities (R. Devine).

Computerized Systems Validation (R. Branning).

Regulation of Pharmaceuticals in Japan (M. Dibner).

Unresolved Issues (T. Copmann & J. Petricciani).

Index.

Erscheint lt. Verlag 30.8.1994
Verlagsort New York
Sprache englisch
Maße 160 x 235 mm
Gewicht 814 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Pharmakologie / Pharmakotherapie
Technik Umwelttechnik / Biotechnologie
ISBN-10 0-471-04900-X / 047104900X
ISBN-13 978-0-471-04900-5 / 9780471049005
Zustand Neuware
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