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Aurigene Pharmaceutical Services Limited vs BioDuro-Sundia

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CategoryAurigene Pharmaceutical Services LimitedBioDuro-Sundia
Listed sitebothcro
SummaryIntegrated CRO-CDMO with 25+ years of discovery and development expertise across small and large molecules, operating 16 US FDA-inspected cGMP facilities across three manufacturing countries.Integrated CRDMO with 30 years of expertise spanning discovery chemistry, biology, DMPK, and IND-enabling development for small and large molecules, plus API and drug product manufacturing.
Services
  • Discovery Research
  • Target Identification & Validation
  • Medicinal Chemistry
  • High-Throughput Screening
  • Computational & In-Silico Drug Discovery
  • Protein Engineering
  • Discovery Research
  • Target Identification & Validation
  • High-Throughput Screening
  • Computational & In-Silico Drug Discovery
  • Medicinal Chemistry
  • In Vitro Pharmacology
  • In Vitro ADME / DMPK
  • Safety Pharmacology
  • Genetic Toxicology
  • Preclinical In Vitro Studies
  • In Vivo Efficacy Models
  • In Vivo PK / PD Studies
  • GLP Toxicology
  • Specialized & Large-Animal Models
  • Preclinical In Vivo Studies
  • Bioanalysis
  • Biomarker Assays
  • Flow Cytometry Services
  • Analytical Method Development & Validation
  • ICH Stability Studies
  • Translational Research
  • US FDA Regulatory Strategy
  • China NMPA Regulatory Strategy
  • Regulatory Affairs
Modalities
  • Small Molecule
  • Biologics (Other)
  • Peptide
  • Small Molecule
  • Biologics (Monoclonal Antibodies)
  • Biologics (Other)
  • Antibody-Drug Conjugate (ADC)
  • Peptide
IndicationsData not yet provided.
  • Oncology
  • Immunology
  • Neurology
  • Metabolic
  • Respiratory
Locations
  • Manufacturing - India, India
  • Manufacturing - UK, United Kingdom
  • Manufacturing - Mexico, Mexico
  • Headquarters, Irvine, California, United States
Certifications
  • FDA · Identifier: 16 US FDA-inspected cGMP facilities
Data not yet provided.
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.