Available: Print or CD
Promotes the development and sharing of
practical drug development knowledge and technology by agency and
industry experts alike.
The world's most definitive & authoritative current generic drug
development series available anywhere.
"very satisfactory - a truly excellent
series"- LEK dd.
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
Edition # and Pub. Year.
H/B Vol 10 - 2010
H/B Vol 11 - 2011
H/B Vol 12 - 2012
H/B Vol 13 - 2013
New Edition Annually
Handbook Generic Development
Analytical
Methods
HPLC SI Generic Drug
Assays
(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.
Complete
Volume ~1150 pp for Part 1 to 4 fully
illustrated
with diagrams, graphs, tables in b/w & color as
a complete volume of four parts.
ISSN:
0793-7756 / 0793-7774
Price:
Locum
International Catalog
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AVAILABILITY
a) Print
b ) Electronic CD - Read only (single user)
c ) Electronic CD - Print (Corporate user)
and may be
d ) Electronic CD - Licenced (Corporate
user)
e ) Electronic CD - Unlicenced
(Corporate
user)
