Available: Print

24 volume Series available as printed hard copy or CD electronic publication (multilicense required)
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.

"Really practical and hands-on... truly excellent formulation know-how -Teva. (on Paracetamol technology)

Vol, Edition # and Pub. Year.

H/B Vol 4/Ed 19 - 2019
H/B Vol 4/Ed 20 - 2020
H/B Vol 4/Ed 21 - 2021
H/B Vol 4/Ed 22 - 2022
H/B Vol 4/Ed 23 - 2023
H/B Vol 4/Ed 24 - 2024
H/B Vol 4/Ed 25 - 2025

New Updated Edition Annually.

Locum Publishers Clients
(Handbooks and Journals

Handbook Generic Development
Oral Imediate Release Liquids

A Two Part Development To Final Production Handbook

Locum International Press

Volume 4 - (Complete Handbook in Two Parts)
of the 24 Volume Drug Development Series.

This Handbook of Pharmaceutical Generic Development is a practical hand-on workbook covering essential liquid formulations such as syrup and sugar-free Paracetamol; Dexchlorpheniramine + Pseudoephedrine; Codine Phosphate + Ephedrine HCl; Pheniramine Maleate; Bromhexine; Oxolamine; Terbutaline; Sodium Valproate and other essential formulations.

It promotes the development and sharing of practical drug development knowledge of liquid dose technology written by government agency and industry experts alike.

Designed to specifically eliminate the potential risks and common process omissions in drug development and claimed as the world's most authoritative and definitive work available on oral dosage form drug development from a generic industry viewpoint.
An Essential Reference for Development Pharmacists, R&D Chemists, QA/QC and Regulatory personnel.

An Essential Reference for Development Pharmacists, R&D Chemists, QA/QC and Regulatory personnel. Each and every document, protocol and procedure in Part I + II is expertly referenced to the appropriate module number in the CTD / e-CTD system thus providing a fully seamless and effortless integration into either US, EU and Asian application files and dossier. All IAGIM technology is purposely and uniquely dove-tailed in regulatory drug product applications -worldwide appliations made simple and precise.

Provide general and specific product development, pre-formulation, formulationa tables, final formulation, stability, scale-up process qualification; pivotal and final validation batches; Analytical, cleaning and process validation; Essential documentation and regulatory know-how that is essential for a successful review for a EU/FDA approval, saving queue-time and money.

Complete Volume in two parts 1690-1850 pp. fully illustrated with diagrams, flow charts, graphs, side-by-side comparisons, tables in b/w & color. Available in print (spiral soft cover) or via digital CD (multi-users require additinal optional license) ISBN: 0793-8756

About Us
Locum International Press are one of the world leading scientific R&D publishers offering an exceptional range of peer reviewed journals, handbooks, book databases and publishing services to the pharmaceutical science community. We also offer a large and comprehensive range of product specific generic handbooks to the pharmaceutical generic drug and innovative drug R&D community.

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