Promotes the development and sharing of practical
drug development knowledge and technology by agency and industry experts
The world's most definitive & authoritative current generic drug development
series available anywhere.
"very satisfactory - a truely excellent series"-
LOCUM INT. PRESS
Vol, Edition # and Pub. Year.
H/B Vol 16/Ed 16 - 2016
H/B Vol 16/Ed 17 - 2017
H/B Vol 16/Ed 18 - 2018
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
New 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
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.
Volume ~1800+ pp fully
with diagrams, graphs, tables in b/w & color.
Price go to: Locum
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