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Aldevron vs Genezen

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CategoryAldevronGenezen
Listed sitecdmocdmo
SummaryAldevron is a CDMO specializing in mRNA manufacturing with LNP encapsulation and fill/finish, viral vector production, plasmid DNA, and gene therapy solutions from discovery through commercialization.Viral vector CDMO specializing in AAV, lentiviral, and retroviral manufacturing for gene and cell therapies, with cGMP facilities in Indiana and Massachusetts supporting preclinical through commercial-scale production.
Services
  • mRNA Manufacturing
  • Lipid Nanoparticle (LNP) Formulation
  • Sterile Fill-Finish & Aseptic Manufacturing
  • Process Development
  • CMC Analytical Development
  • Stability Testing & Storage
  • Quality Control Testing
  • Recombinant Protein Manufacturing
  • Cell-Line Development
  • Lentiviral Vector Manufacturing
  • AAV Manufacturing
  • Viral Vector Manufacturing
  • Technology Transfer
  • CMC Regulatory Submission Support
  • Cell Therapy Manufacturing
  • Cell-Line Development
  • Lentiviral Vector Manufacturing
  • Viral Vector Manufacturing
  • AAV Manufacturing
  • Cell Therapy Manufacturing
  • Stability Testing & Storage
  • Upstream Processing
  • Downstream Processing
  • CMC Analytical Development
  • Quality Control Testing
Modalities
  • mRNA
  • Cell Therapy
  • Gene Therapy
  • Vaccine
  • AAV / Viral Vector Platform
  • Cell Therapy
  • Gene Therapy
  • AAV / Viral Vector Platform
Indications
  • Oncology
  • Metabolic
  • Infectious Disease
  • Rare Disease
Data not yet provided.
Locations
  • Breakthrough Campus (Headquarters), Fargo, North Dakota, USA
  • Advance Campus, Fargo, North Dakota, USA
  • Innovate Campus, Madison, Wisconsin, USA
  • Discovery Center, Waltham, Massachusetts, USA
  • Headquarters
  • Headquarters & Manufacturing, Fishers, Indiana, United States
  • Viral Vector Manufacturing, Lexington, Massachusetts, United States
Certifications
  • Germany (Competent Authority) · Identifier: Certificate of GMP Compliance of a Manufacturer
  • FDA CBER · Identifier: Pre-License Inspection (PLI) and GMP audit - No Action Indicated (NAI)
  • ISO · Identifier: ISO 13485:2016
  • FDA · Identifier: cGMP compliant
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.