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Aurobindo Pharma CDMO vs Grand River Aseptic Manufacturing

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CategoryAurobindo Pharma CDMOGrand River Aseptic Manufacturing
Listed sitecdmocdmo
SummaryAurobindo Pharma Limited is one of the largest generic pharmaceutical companies globally, with a strong commitment to making medicines affordable and accessible.Sterile injectable CDMO specializing in fill-finish services for liquid and lyophilized vials, syringes, and cartridges, with Annex 1 compliant facilities and experience in biologics, small molecules, and vaccines.
Services
  • API Synthesis & Manufacturing
  • Small Molecule Development & Manufacturing
  • Recombinant Protein Manufacturing
  • Biologics Development & Manufacturing
  • Quality Control Testing
  • Stability Testing & Storage
  • Sterile Fill-Finish & Aseptic Manufacturing
  • Vial Filling
  • Prefilled Syringe (PFS) Filling
  • Cartridge Filling
  • Lyophilization (Freeze Drying)
  • Quality Control Testing
  • Secondary Packaging & Labeling
  • Serialization & Track-and-Trace
  • Stability Testing & Storage
  • CMC Analytical Development
  • Technology Transfer
  • CMC Regulatory Submission Support
  • Controlled Substance Manufacturing
  • Vaccine Manufacturing
  • Monoclonal Antibody (mAb) Manufacturing
  • Biologics Development & Manufacturing
  • API Synthesis & Manufacturing
  • Small Molecule Development & Manufacturing
Modalities
  • Biologics (Monoclonal Antibodies)
  • Small Molecule
  • Small Molecule
  • Biologics (Monoclonal Antibodies)
  • Biologics (Other)
  • Vaccine
Indications
  • Oncology
  • Immunology
Data not yet provided.
Locations
  • Registered Office, Hyderabad, Telangana, India
  • Corporate Office, Hyderabad, Telangana, India
  • Kakinada Facility, Kakinada, Andhra Pradesh, India
  • Headquarters, Grand Rapids, Michigan, United States
  • Headquarters
CertificationsData not yet provided.
  • GMP · Identifier: Five GMP manufacturing facilities
  • Annex 1 · Identifier: Three facilities designed and qualified with Annex 1 revisions
  • GMP · Identifier: Five GMP manufacturing facilities; three Annex 1 compliant
  • FDA · Identifier: GMP
  • EMA · Identifier: Annex 1
  • GMP · Identifier: Five GMP manufacturing facilities (three Annex 1 compliant)
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.