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Handbook of pharmaceutical biotechnology

By: Contributor(s): Material type: TextTextPublication details: New Delhi Viva Books 2004Description: xi, 191pISBN:
  • 9788176497855
  • 8176497851
Subject(s): DDC classification:
  • 660.6 RHO-H
Summary: Stay up to date with changes in the biopharmaceutical products market with the growth rate of biopharmaceutical products ascending rapidly since the 1980s, the number of Biotechnology companies has risen to more than 1200 new businesses in the unites stat.Summary: Comprehensive professional reference handbook providing a practical overview of all approaches to discovering, selecting, and producing biotechnology- derived drugs. Fifty chapters by leading industry practitioners span the full drug development lifecycle: bioinformatics and pharmacogenomics; toxicogenomics; preclinical pharmacokinetics; macromolecule manufacturing and process validation; stability and formulation; protein modification and PEGylation; delivery systems; biologics development; regulatory affairs. Essential reference for pharmaceutical scientists, toxicologists, biochemists, molecular biologists, formulation chemists, and QA/QC professionals.
Item type: Reference
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Item type Current library Home library Call number Materials specified Status Date due Barcode
Reference Central Library, NIT Jalandhar Reference Central Library, NIT Jalandhar 660.6 RHO-H (Browse shelf(Opens below)) Not for loan 87867

Stay up to date with changes in the biopharmaceutical products market with the growth rate of biopharmaceutical products ascending rapidly since the 1980s, the number of Biotechnology companies has risen to more than 1200 new businesses in the unites stat.

Comprehensive professional reference handbook providing a practical overview of all approaches to discovering, selecting, and producing biotechnology- derived drugs. Fifty chapters by leading industry practitioners span the full drug development lifecycle: bioinformatics and pharmacogenomics; toxicogenomics; preclinical pharmacokinetics; macromolecule manufacturing and process validation; stability and formulation; protein modification and PEGylation; delivery systems; biologics development; regulatory affairs. Essential reference for pharmaceutical scientists, toxicologists, biochemists, molecular biologists, formulation chemists, and QA/QC professionals.

Dr. Sanjeev, Librarian
Managed by: Dr. D. P. Tripathi, Deputy Librarian, Central Library
For any query / question, please mail at circulation.liby@nitj.ac.in 

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