Enteris supports clients through all stages of development for solid oral dosage forms, from formulation and analytical method development to clinical and commercial cGMP manufacturing.

Our 32,000 square foot state-of-the-art cGMP facility is equipped to handle a myriad of APIs, including dedicated processing and containment areas for highly potent API (HPAPI). We provide total integrated CMC support, including preformulation, formulation, analytical R&D, quality control & quality assurance, clinical & commercial manufacturing, and regulatory assistance.

Our clients have direct access to our CMC experts, allowing for rapid problem solving, specialized project management, and efficient project completion.

KNOWLEDGE CENTER

Expand your knowledge. The Enteris BioPharma Knowledge Center is a library of educational tools.

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KNOWLEDGE CENTER

Expand your knowledge. The Enteris BioPharma Knowledge Center is a library of educational tools.

LEARN MORE