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.

"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

Vol, Edition # and Pub. Year.

H/B Vol 13/Ed 18 - 2018
H/B Vol 13/Ed 19 - 2019
H/B Vol 13/Ed 20 - 2020
H/B Vol 13/Ed 21 - 2021
H/B Vol 13/Ed 22 - 2022
H/B Vol 13/Ed 23 - 2023
H/B Vol 13/Ed 24 - 2024

New Updated Edition Annually

Handbook Generic Development
Analytical Methods
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.

Complete Volume ~1800 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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