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Bioavailability and bioequivalence in pharmaceutical technology / edited by Tapan Kumar Pal and M. Ganesan

Contributor(s): Material type: TextTextPublication details: New Delhi, India : CBS Publishers & Distributors, c2004Description: viii, 159 pages : illustrations ; 25 cmISBN:
  • 8123911580
Subject(s): LOC classification:
  • RS 192 .B56 2004
Contents:
Ethical issues involved in Bioequivalence study -- Understanding bioavailability -- Bioavailability studies in man: pharmacokinetic considerations -- Method of sample preparation and HPLC analysis of some common drugs from biological fluids -- Application of HPLC for analysis of biological samples and drugs -- Microdialysis and its application in bioavailability studies -- Ocular kinetics and drug delivery systems of ophthalmic medicines- a review -- Bioequivalence study and data interpretation -- Introduction to bio-analytical method development and validation for bioavailability and bio-equivalence studies -- High performance liquid chromatography, an upgraded technology for the monitoring of therapeutic drugs -- Systematic clinical and toxicological analysis using solid phase extraction -- Bioequivalence of Gatifloxacin by HPLC method- a case study
Summary: Proceedings of the Seminar-cum-Workshop on Bioavailability and Bioequivalence.
Item type: Books
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Holdings
Item type Current library Home library Collection Call number Copy number Status Date due Barcode
Books Books National University - Manila LRC - Main General Circulation Pharmacy GC RS 192 .B56 2004 (Browse shelf(Opens below)) c.1 Available NULIB000004004

Includes bibliographical references.

Ethical issues involved in Bioequivalence study -- Understanding bioavailability -- Bioavailability studies in man: pharmacokinetic considerations -- Method of sample preparation and HPLC analysis of some common drugs from biological fluids -- Application of HPLC for analysis of biological samples and drugs -- Microdialysis and its application in bioavailability studies -- Ocular kinetics and drug delivery systems of ophthalmic medicines- a review -- Bioequivalence study and data interpretation -- Introduction to bio-analytical method development and validation for bioavailability and bio-equivalence studies -- High performance liquid chromatography, an upgraded technology for the monitoring of therapeutic drugs -- Systematic clinical and toxicological analysis using solid phase extraction -- Bioequivalence of Gatifloxacin by HPLC method- a case study

Proceedings of the Seminar-cum-Workshop on Bioavailability and Bioequivalence.

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