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Akums Drugs and Pharmaceuticals Ltd. vs Ascendiacdmo

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CategoryAkums Drugs and Pharmaceuticals Ltd.Ascendiacdmo
Listed sitecdmocdmo
SummaryIndia's largest CDMO with 15+ state-of-the-art facilities and 30% domestic market share, manufacturing 4,100+ formulations across tablets, capsules, injectables, APIs, and specialty dosage forms under WHO-GMP, USFDA, EU-GMP, and TGA compliance.Ascendia is a specialty CDMO offering formulation development, analytical services, and cGMP manufacturing for small molecules, biologics, and gene delivery therapies, with proprietary nanotechnologies for solubility and bioavailability enhancement.
Services
  • Formulation Development
  • Process Development
  • Technology Transfer
  • CMC Regulatory Submission Support
  • CMC Analytical Development
  • Stability Testing & Storage
  • Quality Control Testing
  • Oral Solid Dosage Manufacturing
  • Ophthalmic Manufacturing
  • Inhalation & Nasal Dosage Manufacturing
  • Topical & Semi-Solid Manufacturing
  • Vial Filling
  • Lyophilization (Freeze Drying)
  • Sterile Fill-Finish & Aseptic Manufacturing
  • API Synthesis & Manufacturing
  • Formulation Development
  • CMC Analytical Development
  • Stability Testing & Storage
  • Process Development
  • Technology Transfer
  • CMC Regulatory Submission Support
  • Oral Solid Dosage Manufacturing
  • Lyophilization (Freeze Drying)
  • Vial Filling
  • Sterile Fill-Finish & Aseptic Manufacturing
  • Prefilled Syringe (PFS) Filling
Modalities
  • Small Molecule
  • Biologics (Other)
  • Small Molecule
  • Biologics (Other)
  • Gene Therapy
Indications
  • Ophthalmology
  • Respiratory
  • Dermatology
Data not yet provided.
Locations
  • Sterile Manufacturing Facility, Haridwar, India
  • Headquarters & Manufacturing, New Jersey, New Jersey, United States
Certifications
  • WHO · Identifier: WHO-GMP
  • FDA · Identifier: USFDA
  • EMA · Identifier: EU-GMP
  • TGA · Identifier: TGA
Data not yet provided.
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.