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Imaginative chemical modelling facilitating drug discovery |
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Overview Trinity Laboratories, Inc. is acknowledged as an
industry leader in rapid, high quality sterile drug product development.
Our 10,000 square foot cGMP research & development facilities are capable
of performing a wide range of drug development activities. This includes
active pharmaceutical ingredient qualification, analytical methods development
and validation, product stability storage and monitoring, analytical testing
and drug product dossier development and submission. |
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Trinity's advanced workspace unifies bench and computerized components, as well as tools for descriptor calculation, fragmental and statistical analysis.
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