Scientific rigor
Frame a clear question, select an appropriate approach and interpret evidence within its limits.
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From its beginnings in North Carolina, SmaBio Labs has brought scientific curiosity and practical development expertise together around the needs of drug development teams.
Explore our journey
Advance drug development through scientific rigor, responsive collaboration and a clear understanding of the product question. Connect formulation, analytical insight and clinical-stage requirements around the next development decision.
SmaBio Labs was founded in Apex, North Carolina, beginning in a 2,000-square-foot space.
The published company timeline records a move to a 10,000-square-foot RTP facility supporting early-phase GMP manufacturing.
The company timeline identifies FDA registration of its analytical laboratory as a milestone in its development. Registration is not FDA approval of a drug product.
The existing website describes a potential expansion in Research Triangle Park. This is a forward-looking milestone and does not establish that a facility is qualified or that commercial manufacturing is operational.
Formulation development, analytical services, stability and clinical trial material capabilities provide several points of entry for a scientific conversation. Each project begins with review of fit and scope.
Frame a clear question, select an appropriate approach and interpret evidence within its limits.
Make assumptions, dependencies and open questions part of the technical discussion.
Agree responsibilities, documentation and deliverables before the work begins.
Work with teams nearby, across the United States and internationally around the product objective.
Share your product, scientific challenge and next milestone. Request an NDA before providing proprietary details.