End-to-End Program
End-to-End Program
ISSUE NO. 27 — The Complexities of Early-Phase Ophthalmic Drug Development
One Integrated Solution for Meeting Your Preclinical to Clinical Drug Development Needs
Five Things You Need to Know About Partnering with an Integrated CRO/CDMO
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We are often asked about the advantages of working with an integrated CRO/CDMO.
Five Ways Altasciences Simplifies the Drug Development Process for You
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Bringing new drugs to market, from lead candidate selection through preclinical testing, to clinical proof of concept, is a complex, time-consuming, and costly process.
Making Early-Phase Drug Development Faster, Better, and More Efficient
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Early-phase drug discovery and drug development are complex processes, where many moving parts can, and do, influence the success of a program.
ISSUE NO. 6 — Hybrid Medicines and 505(b)(2) NDA Approval Pathways
Hybrid medicines are drugs based on a generic molecule, and have a different route of administration, format, strength, or indication from the original reference product.
They require re-approval for market authorization, partly based