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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 truely excellent series"- LEK dd.

Vol, Edition # and Pub. Year.

H/B Vol 16/Ed 19 - 2019
H/B Vol 16/Ed 20 - 2020
H/B Vol 16/Ed 21 - 2021
H/B Vol 16/Ed 22 - 2022
H/B Vol 16/Ed 23 - 2023
H/B Vol 16/Ed 24 - 2024
H/B Vol 16/Ed 25 - 2025
H/B Vol 16/Ed 26 - 2026

New updated Edition Annually.

Locum Publishers Clients
(Handbooks and Journals)

Handbook Generic Development
Oral Tablets Complete (All dosage forms)

A Four
Part Development To Final Production Handbook
All oral dosage forms with Development + Expert Reports

Locum International Press.

Volume 16 - [IR / CR / MR / DR / Chew + Expert and Development Reports]
24 Volume Drug Development Series.

This handbook claimed as the world's most authoritative and definitive work available on immediate, modified to extended and delayed oral dosage forms (five forms) of drug development from the pharmaceutical industry viewpoint. An Essential Reference for development pharmacists, R&D chemists, QA/QC and regulatory personnel on Immediate (IR), Chew (IRC), Controlled (CR), Delayed (DR)and Modified Release (MR) dosage forms.

Master Formula and detailed step-by-step processes of current US and EU commercial drug product leaders.
Essential development and submission know-how on all forms of Oral Chew and Oral IR MR, DR and CR Tablets technology for professional drug developers and review authorities to understand the nuts-and-bolts of drug development with an emphasis on high-tech detailed commercial product know-how.

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 applications made simple and precise.

Essential development and submission know-how on chew and Oral IR, Oral MR, Oral DR and Oral CR Tablets for the professional drug developer to really understand the nuts-and-bolts of drug development with a high-tech integrated formulation charts, unique and advanced developmental procedures, development and manufacturing flowcharts, decision trees, production tables, master formula and detailed manufacturing processes, development and production SOPs, production, validation and cleaning checklists and much, much more.

Complete Volume ~1800+ pp fully illustrated with diagrams, graphs, tables in b/w & color.

ISSN: 0793-7856 / 0793-7884

Price go to: Locum International Catalog

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