Regis Custom Pharma is a US-based contract development and manufacturing organization (CDMO) focused on the development and manufacture of NCE’s (New Chemical Entities). We offer a comprehensive range of drug substance development services including Process Chemistry, Analytical Method Development and Validation, Solid State Chemistry , Micronization, cGMP Manufacturing, Process Validation, and Stability Services.
Over the last 65 years, Regis has a successful history of supporting the development of hundreds of new drug candidates. Many programs have entailed Process Optimization, Process Registration, and Validation. Today, we manufacture drug substance for both clinical use and the commercial market.
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