cdmo.directory
← Compare landing

Codis vs Optimus Drugs Private Limited

Auto-generated comparison by BioBM Editorial AI. This page highlights available profile evidence side by side and avoids drawing conclusions from missing fields.

Markdown mirror: /api/markdown/compare/codis/optimuspharma

CategoryCodisOptimus Drugs Private Limited
Listed sitecdmocdmo
SummaryGlobal 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.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
  • Quality Control Testing
  • CMC Regulatory Submission Support
  • Oral Solid Dosage Manufacturing
  • Secondary Packaging & Labeling
  • 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
  • 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
  • Headquarters, India
Certifications
  • FDA · Identifier: 21 CFR 210/211, 110/111, 117
  • German Authorities · Identifier: Manufacturing site GMP approval (Pharmaceutical Products Act)
  • 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.