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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
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
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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