Nivagen Pharmaceuticals Inc. is a full-scale Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. Nivagen can serve customers globally from our integrated facility in Sacramento, California. Nivagen can offer a comprehensive range of services, including drug discovery solutions, process and pharmaceutical development services, clinical trial supplies, and commercial supply of finished dosage forms of sterile injectables.
As part of our CDMO services, we provide Visual Inspection to help clients comply with diverse regulations. We ensure our clients’ products meet the stringent standards of the market.
From cartridges to vials, our visual inspection services encompass a wide range of sterile products, ensuring compliance and safety.
From cartridges to vials, our visual inspection services encompass a wide range of sterile products, ensuring compliance and safety.
Our packaging facilities specialize in delivering innovative, secure, and compliant packaging solutions tailored to your unique product range. We offer a wide selection of packaging options that comply with international pharmaceutical regulations and are specifically customized to your needs.
At Nivagen, our cutting-edge R&D facility in the California, is the driving force behind our innovative drug development initiatives. Spanning over 9,000 square feet, this facility is equipped with the latest technologies to support our research and development efforts.
Nivagen has a c-GMP sterile injectables facility spanning 100,000 sq ft in Sacramento, CA, USA with the aim of expanding CDMO services and 503B products to address FDA shortages.
