Promotes the development and sharing of
practical drug development knowledge and technology by agency and industry
The world's most definitive & authoritative current generic drug
development series available.
"very satisfactory - a truly excellent series"-
Great analytical, process validations and protocol -
our system uses these workable models - TEVA US
The handbook meets our validation needs from analytical
to final product - IVAX
LOCUM INT. PRESS
Vol, Edition # and Pub. Year.
H/B Vol 13/Ed 14 - 2014
H/B Vol 13/Ed 15 - 2015
H/B Vol 13/Ed 16 - 2016
H/B Vol 13/Ed 17 - 2017
H/B Vol 13/Ed 18 - 2018
H/B Vol 13/Ed 19 - 2019
H/B Vol 13/Ed 20 - 2020
New Edition Annually
HPLC SI Generic Drug Assays
Locum International Press.
Volume 13 - (Part
I - 4)
24 Volume Drug Development Series.
A four volume analytical and validation handbook claimed as the world's
most authoritative and definitive work available on analytical methodology
of drug development from a generic and innovative industry's viewpoint.
An essential laboratory reference no lab should be without, for drug researchers
development pharmacists, method and validation procesure analytical 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 know-how
of the most important drugs of the 21 millennium.
For professional generic assay 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 ~1800 pp for Part 1 to 4 fully
with diagrams, graphs, tables in b/w & color as
a complete volume of four parts.
| Handbook Series | Journal
Index | Specialized Journals