READY-TO-GO CMC &
HANDBOOK SERIES
The
Differences - From Production CMC to Authoritative
References
Ready-To-Go
CMC Title 21 Series
|
Ready-To-Go
Title 19 Handbooks
|
|
Title
21 - ' Just Production '
|
Title
19 - ' The
Full
Reference Work'
|
|
The product database is based
on the CMC information found in an existing commercial US file or
and EU Dossier and saves many months of product development - eliminating
costly drug development, tedious analytical development and validation,
pre-formulation, formulation, optimization, scale-up, written protocols,
stability and process qualification as well as many aspects of analytical
and process validation. |
The Title 19 Handbooks are
more significantly more detailed and complete reference works and
include extensive drug development work of the specific generic product
- including content uniformity qualification and/or hardness range
and dissolution profiles for tablets as appropriate. |
|
TITLE 21 - CMC | TITLE 19 - HANDBOOKS | |
TITLE COMPARISON Above description shows the differences between the two references series - designed for different personnel, reference and research uses. Title 19 is designed for Drug Development to Commercial Validated Batches (from A-Z) - while Title 21 contains standard plant know-how database technology similar to a CMC technology transfer and is a more cost effective purchase. Title 21 are designed for in-house continual development and are available to IAGIM members at 2-3 products per month as the latest data becomes available to IAGIM research laboratories. All IAGIM research is solely for specific membership development use only under copyright and not for resale to nonmember third parties or countries. |
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