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
Handbook Generic Development
HPLC SI Generic Drug Assays (Part
I - 5)
A Five Part Series
Locum International Press.
Advanced Level Volume 13E - (Parts
I - 5)
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. Advanced biopharma glatiramer
acetate analytical methodogy impurities and molecular weight indicating
methodology using S12 gel filtration and reverse HPLC techniques adjusting
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.
Designed 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 up to ~1900 pp for Part 1 to 5 fully
with diagrams, graphs, tables in b/w & color as
a complete volume of four parts).
Price go to: Locum
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