CoJourney Co.
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CoJourney CO. is reimagining cell and gene therapy CDMO services globally. Our platform is built on High Purity, High Yield, On Time Supply and Significantly Reduced Costs. We provide process development and clinical and commercial mfg. through a range of platform technologies, including: (1) Plasmids, (2) mRNA, (3) AAV / adenovirus, (4) Lentivirus, (5) Retrovirus, (6) Custom Viral Vectors.
We have proprietary high-purity, high-yield, streamlined and cost-effective processes and our facilities are compliant under US FDA, EU EMA and China NMPA Plasmid, mRNA, and Viral Vector development, manufacturing and import/export regulations.
Plasmids are manufactured in a multi-product cGMP facility that includes multiple upstream suites, downstream suites and a fill-finish suite with an isolator and filler. The facility includes 30L disposable fermenters for plasmid production.
Viral Vectors are manufactured in a cGMP viral vector facility that includes multiple upstream cell culture, upstream viral vector production suites, downstream processing and fill-finish suites. The facility includes 500L and 2,000L disposable bioreactors for viral vector production.
CoJourney’s Process Development labs allow separate, client specific project rooms and are equipped with state of the art and large-scale equipment. The analytical development and Quality Control laboratories provide state of the art analytical equipment are focused on analytical development and performing all stages of release testing for plasmids and viral vectors.
CoJourney is currently manufacturing AAV-based gene therapies that have been approved for use in global clinical trials:
1) rAAV based gene therapy for Neurovascular Age-Related Macular Degeneration (wet AMD) in USA
2) AAV based gene therapy for Spinal Muscular Atrophy (SMA) in China
Please contact us to discuss how our innovative approaches and timely, cost-effective solutions can address your needs.
Please contact us for more information.
We have proprietary high-purity, high-yield, streamlined and cost-effective processes and our facilities are compliant under US FDA, EU EMA and China NMPA Plasmid, mRNA, and Viral Vector development, manufacturing and import/export regulations.
Plasmids are manufactured in a multi-product cGMP facility that includes multiple upstream suites, downstream suites and a fill-finish suite with an isolator and filler. The facility includes 30L disposable fermenters for plasmid production.
Viral Vectors are manufactured in a cGMP viral vector facility that includes multiple upstream cell culture, upstream viral vector production suites, downstream processing and fill-finish suites. The facility includes 500L and 2,000L disposable bioreactors for viral vector production.
CoJourney’s Process Development labs allow separate, client specific project rooms and are equipped with state of the art and large-scale equipment. The analytical development and Quality Control laboratories provide state of the art analytical equipment are focused on analytical development and performing all stages of release testing for plasmids and viral vectors.
CoJourney is currently manufacturing AAV-based gene therapies that have been approved for use in global clinical trials:
1) rAAV based gene therapy for Neurovascular Age-Related Macular Degeneration (wet AMD) in USA
2) AAV based gene therapy for Spinal Muscular Atrophy (SMA) in China
Please contact us to discuss how our innovative approaches and timely, cost-effective solutions can address your needs.
Please contact us for more information.
CoJourney Co. Offices
OnSite Workspace
Employees work from physical offices.
Typical time on-site:
None
Philadelphia, Pennsylvania, USA
