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Codis vs Medpharm

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CategoryCodisMedpharm
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.Specialized CDMO for topical, transdermal, and transepithelial drug products offering formulation development, analytical testing, process scale-up, and GMP manufacturing from early development through commercialization.
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
  • Formulation Development
  • CMC Analytical Development
  • Stability Testing & Storage
  • Process Development
  • Technology Transfer
  • Topical & Semi-Solid Manufacturing
  • Ophthalmic Manufacturing
  • Inhalation & Nasal Dosage Manufacturing
  • Secondary Packaging & Labeling
  • Serialization & Track-and-Trace
  • Quality Control Testing
Modalities
  • Small Molecule
  • Small Molecule
IndicationsData not yet provided.
  • Dermatology
  • Ophthalmology
  • Respiratory
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, Guildford, England, United Kingdom
  • US Operations, Durham, North Carolina, United States
Certifications
  • FDA · Identifier: 21 CFR 210/211, 110/111, 117
  • German Authorities · Identifier: Manufacturing site GMP approval (Pharmaceutical Products Act)
Data not yet provided.
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.