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CMC Pharmaceuticals, Inc. vs UPM Pharmaceuticals

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CategoryCMC Pharmaceuticals, Inc.UPM Pharmaceuticals
Listed sitecdmocdmo
SummaryCMC Pharma provides integrated formulation development, analytical testing, stability studies, and cGMP manufacturing oversight for small molecule drug programs from preclinical through post-approval, with hands-on regulatory expertise and CMO management built in.Independent, family-owned CDMO specializing in oral solids, semi-solids, and controlled-substance manufacturing with 475,000 sq ft cGMP facility in Bristol, TN; over 80 products commercialized.
Services
  • Formulation Development
  • Process Development
  • CMC Analytical Development
  • Stability Testing & Storage
  • Quality Control Testing
  • Technology Transfer
  • CMC Regulatory Submission Support
  • API Synthesis & Manufacturing
  • Small Molecule Development & Manufacturing
  • Controlled Substance Manufacturing
  • HPAPI Manufacturing (High-Potency)
  • Formulation Development
  • CMC Analytical Development
  • Stability Testing & Storage
  • Quality Control Testing
  • Process Development
  • Technology Transfer
  • Oral Solid Dosage Manufacturing
  • Topical & Semi-Solid Manufacturing
  • Secondary Packaging & Labeling
  • Serialization & Track-and-Trace
  • Controlled Substance Manufacturing
  • HPAPI Manufacturing (High-Potency)
Modalities
  • Small Molecule
  • Small Molecule
IndicationsData not yet provided.Data not yet provided.
Locations
  • Headquarters, Solon, Ohio, United States
  • Headquarters & Manufacturing Facility, Bristol, Tennessee, United States
CertificationsData not yet provided.Data not yet provided.
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.