NextPharma San Diego offers cGMP contract manufacturing services to the biotechnology, medical device and pharmaceutical industries.

Our knowledgeable scientists have extensive experience in all aspects of manufacturing, including scale-up and process development, final formulation and product filling. Our facility has been designed with flexibility in mind to accommodate a broad spectrum of cGMP manufacturing services, including the manufacturing of preclinical, Phase I and Phase II clinical products containing biologics (e.g., proteins, oligonucleotides, etc.) or small molecules, in liquid, semi-solid, lyophilized, or powder form filled aseptically or non-aseptically into vials, bottles, IV bags, tubes or syringes.

Our experienced Quality Assurance team oversees all aspects of the process and work closely with our customers to ensure that all US regulatory requirements are met. We are FDA registered and inspected as well as ISO Certified [ISO13485:2003 (Certificate Number FM77429)].