Drug Product
Formulation, Analytical and Process Development
Clinical Trial Material Manufacturing (Phase 0 - III)
Validation, Registration, and Commercial Manufacturing

Oral Dose:

Bioavailability Enhancement: Spray Dried Dispersion and Hot Melt Extrusion

Modified Release Formulations (delayed, sustained, and custom release)

Immediate Release (Tablets, Capsules, min-tablets)

Controlled Drug Substances (schedules I-V)

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