HPLC SI Generic Drug
(Part I - 4)
Locum International Press.
Volume 13 - (Parts 1 to 4)
of the 24 Volume Drug Development Series.
Over five years in preparation and claimed as the world's most authoritative
and definitive work available on analytical methodology of drug development
from a generic industry's viewpoint.
An Essential Reference for development pharmacists, method developers,
R&D chemists, QA/QC and regulatory personnel.
HPLC, UV and GC detailed step-by-step stability indicating methods of
current US and EU commercial generic drug products . Essential analytical
validation know-how on assays, dissolution and impurity profiles knowhow
of the most important drugs of the 21 millennium.
For professional generic analytical HPLC method developers to understand
the nuts-and-bolts on generic method development with a high-tech detailed
working procedures and state-of-the-art methodology.
Volume ~1150 pp for Part 1 to 4 fully
with diagrams, graphs, tables in b/w & color as
a complete volume of four parts.
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