PacificGMP is a Contract Manufacturing Organization (CMO) and leader in the industry in single-use technology for development and manufacturing of biologics. Our team has extensive experience in process development and production of antibodies, recombinant proteins, vaccines and cell therapy products. PacificGMP assists its client partners through the early stages of process design, development and scale-up, preclinical and clinical manufacturing, product purification and fill and finish.
cGMP and non-cGMP Services
PacificGMP provides an array of cGMP and non-GMP production services for recombinant proteins, antibodies, vaccines and cell therapies for preclinical and clinical materials. Our technology and expertise allow for rapid turnaround times and the most cost effective solutions in the industry.
Process Development
PacificGMP excels at upstream and downstream process development. Process development services can stand alone or be integrated into preclinical and clinical manufacturing projects. PacificGMP focuses on improving yield at each stage of development by optimizing each step in the process.
Regulatory Affairs Compliance
PacificGMP specializes in the manufacture of proteins, gene therapy vectors, and cellular therapies. Our staff is well-versed in the guidelines of current Good Manufacturing Procedures, in particular as they apply to the manufacture of biologic agents, as well as Good Tissue Practices. PacificGMP also adheres to international GMP requirements as set forth by the International Conference on Harmonization guidelines and related documents.
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