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USA-based CDMO specializing in lyophilization R&D, formulation development, and small-batch manufacturing for pharma and diagnostics. ISO 13485 and ISO 9001 certified with 35+ years of industry experience.

Fee-for-service CDMO specializing in formulation development, process development, and GMP manufacturing of oral dosage forms from preclinical through Phase II, with proprietary KinetiSol amorphous solid dispersion technology for poorly soluble APIs.
Sponsorship inventory available · See packages & pricing