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Alcami Corporation vs Lupin Limited

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CategoryAlcami CorporationLupin Limited
Listed sitecdmocdmo
SummaryUS-based CDMO with 45+ years of experience providing integrated lab services, sterile and oral solid dose drug product manufacturing, and cGMP pharmaceutical storage and support services.Global pharmaceutical manufacturer with robust quality systems aligned to US FDA, UK MHRA, and EU GMP standards; operates diversified manufacturing across generics, complex formulations, and specialty segments with advanced automation and digital quality infrastructure.
Services
  • Sterile Fill-Finish & Aseptic Manufacturing
  • Oral Solid Dosage Manufacturing
  • CMC Analytical Development
  • Formulation Development
  • Quality Control Testing
  • Extractables & Leachables Studies
  • Stability Testing & Storage
  • CMC Regulatory Submission Support
  • Technology Transfer
  • Secondary Packaging & Labeling
  • Quality Control Testing
  • Stability Testing & Storage
  • CMC Regulatory Submission Support
  • Technology Transfer
  • Formulation Development
  • Process Development
  • Inhalation & Nasal Dosage Manufacturing
  • Oral Solid Dosage Manufacturing
  • Sterile Fill-Finish & Aseptic Manufacturing
  • CMC Analytical Development
  • Combination Product Assembly & Final Packaging
ModalitiesData not yet provided.
  • Small Molecule
  • Biologics (Monoclonal Antibodies)
  • Biologics (Other)
IndicationsData not yet provided.
  • Gastroenterology
  • Metabolic
Locations
  • Headquarters, North Carolina, United States
  • Headquarters, Mumbai, Maharashtra, India
  • Global presence, Multiple
  • Global presence, Multiple (100+ countries)
  • Global Operations, Multiple (100+ countries)
  • Global, Multiple (100+ countries)
CertificationsData not yet provided.
  • US FDA · Identifier: FDA-compliant manufacturing sites
  • EMA · Identifier: EU GMP-aligned operations
  • UK MHRA · Identifier: UK MHRA-aligned regulatory systems
  • FDA · Identifier: US FDA
  • EMA · Identifier: EU GMP
  • MHRA · Identifier: UK MHRA
  • US FDA · Identifier: US FDA
  • UK MHRA · Identifier: UK MHRA
  • EU GMP · Identifier: EU GMP
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.