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Bend Bioscience vs Optimus Drugs Private Limited

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CategoryBend BioscienceOptimus Drugs Private Limited
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.Leading CDMO delivering end-to-end small molecule drug substance and drug product development and manufacturing from clinical to commercial scale, with 21+ years of expertise and GMP-certified 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
  • CMC Analytical Development
  • Topical & Semi-Solid Manufacturing
  • Quality Control Testing
  • Stability Testing & Storage
  • API Synthesis & Manufacturing
  • Small Molecule Development & Manufacturing
  • Process Development
  • Formulation Development
  • Oral Solid Dosage Manufacturing
  • Technology Transfer
  • CMC Regulatory Submission Support
Modalities
  • Small Molecule
  • Small Molecule
IndicationsData not yet provided.
  • Metabolic
  • Cardiovascular
  • Neurology
  • Infectious Disease
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
  • Headquarters, India
CertificationsData not yet provided.
  • US FDA · Identifier: FDA approval (FDF facility)
  • EMA · Identifier: EU GMP approval
  • ANVISA · Identifier: ANVISA audit clearance (Unit 1)
  • WHO · Identifier: WHO GMP audit clearance
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.