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Bend Bioscience vs Experic

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CategoryBend BioscienceExperic
Listed sitecdmocdmo
SummaryU.S. pharmaceutical CDMO offering design, development, and manufacturing of oral solid and liquid dosage forms, from early formulation to commercial-scale production across three domestic locations.Specialist powder-handling CDMO offering clinical trial supply, development, manufacturing, and packaging services for pharmaceutical products.
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
  • Process Development
  • CMC Analytical Development
  • Formulation Development
  • Inhalation & Nasal Dosage Manufacturing
  • Secondary Packaging & Labeling
  • Serialization & Track-and-Trace
  • Quality Control Testing
  • Technology Transfer
  • Cold-Chain Storage & Logistics
  • Combination Product Assembly & Final Packaging
Modalities
  • Small Molecule
Data not yet provided.
IndicationsData not yet provided.Data not yet provided.
Locations
  • Bend, Bend, Oregon, United States
  • Georgia, Georgia, United States
  • Florida, Florida, United States
  • Clearwater, Clearwater, Florida, United States
  • Gainesville, Gainesville, Georgia, 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
  • US Facility, United States
  • EU Facility, European Union
  • EU Facility, Europe
CertificationsData not yet provided.
  • FDA · Identifier: 21 CFR Parts 210, 211, 820
  • ICH · Identifier: Q7, Q9, Q10
  • EMA · Identifier: EudraLex Volume 4
  • ISO · Identifier: 13485:2016
  • DEA · Identifier: Schedules I–V
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.