Manufacturing And Analytical Services

Our team provides comprehensive drug development, manufacturing, and analytical services to pharmaceutical and biotech companies worldwide. Capabilities span formulation development, Phase 1 through commercial-scale manufacturing, and ICH stability, storage, and testing.

We offer analytical method development, qualification, and validation, along with finished product and release testing to ensure quality and compliance. Backed by a DEA manufacturing and analytical license (Schedules 1–5), we have formulated, tested, and manufactured nearly every dosage form on the market — including tablets, liquid and powder-filled capsules, over-encapsulated capsules, nanomilled suspensions, creams, gels, powders, and terminally sterilized injectables.

Our purpose-built facility features state-of-the-art Grade C and D cleanrooms, R&D and formulation labs, ICH stability chambers, a cGMP warehouse, and global shipping capabilities — supporting every stage of your program with precision, scalability, and speed.