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Bend Bioscience vs Codis

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CategoryBend BioscienceCodis
Listed sitecdmocdmo
SummaryU.S. pharmaceutical CDMO offering design, development, and manufacturing from early formulation to commercial-scale production, with cGMP capabilities including spray drying, particle engineering, and complex oral dosage forms.Global CDMO specializing in commercial-scale spray drying, amorphous solid dispersions, microencapsulation, and continuous granulation with 400,000 sq ft of GMP manufacturing across US and UK facilities.
Services
  • Formulation Development
  • Process Development
  • CMC Analytical Development
  • Stability Testing & Storage
  • Technology Transfer
  • Secondary Packaging & Labeling
  • Quality Control Testing
  • Oral Solid Dosage Manufacturing
  • Inhalation & Nasal Dosage Manufacturing
  • Topical & Semi-Solid Manufacturing
  • Sterile Fill-Finish & Aseptic Manufacturing
  • CMC Regulatory Submission Support
  • Formulation Development
  • Process Development
  • CMC Analytical Development
  • Stability Testing & Storage
  • Quality Control Testing
  • CMC Regulatory Submission Support
  • Oral Solid Dosage Manufacturing
  • Secondary Packaging & Labeling
Modalities
  • Small Molecule
  • Small Molecule
IndicationsData not yet provided.Data not yet provided.
Locations
  • Bend, Bend, Oregon, United States
  • Georgia, Georgia, United States
  • Florida, Florida, United States
  • Headquarters / Manufacturing, Bend, Oregon, United States
  • Operations, Georgia, Georgia, United States
  • Operations, Florida, Florida, United States
  • Headquarters, Bend, Oregon, United States
  • Office, Georgia, Georgia, United States
  • Office, Florida, Florida, United States
  • Headquarters, St. Louis, Missouri, USA
  • Microencapsulation & Continuous Granulation, St. Louis, Missouri, USA
  • Spray Drying & Commercial Manufacturing, Haverhill, England, UK
  • Manufacturing Facility, Nottingham, England, UK
  • Manufacturing Facility, Seymour, Indiana, USA
CertificationsData not yet provided.
  • FDA · Identifier: 21 CFR 210/211, 110/111, 117
  • German Authorities · Identifier: Manufacturing site GMP approval (Pharmaceutical Products Act)
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.