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Altasciences vs Certara

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CategoryAltasciencesCertara
Listed sitebothcro
SummaryMid-size early phase CRO/CDMO in Canada and the U.S. offering preclinical safety testing, clinical pharmacology (Phase I–II), bioanalysis, research services, and manufacturing with integrated capabilities.Certara transforms drug development with proprietary biosimulation software, predictive modeling, and AI-driven services spanning discovery through commercialization. Serving 2,400+ biopharmaceutical companies and regulatory agencies across 70 countries, Certara's model-informed drug development (MIDD) platform accelerates clinical and regulatory decision-making.
Services
  • Preclinical In Vivo Studies
  • GLP Toxicology
  • Safety Pharmacology
  • In Vitro Pharmacology
  • Phase I Clinical Trials
  • Phase II Clinical Trials
  • Clinical Trial Services
  • Bioanalysis
  • Ligand-Binding Bioanalysis (Large Molecule)
  • Analytical Method Development & Validation
  • ICH Stability Studies
  • Biostatistics & Statistical Programming
  • Data Management & eClinical
  • Medical Writing
  • Clinical Operations
  • Regulatory Affairs
  • In Vivo PK / PD Studies
  • Preclinical In Vitro Studies
  • Phase IV / Post-Marketing
  • In Vitro ADME / DMPK
  • Formulation Development
  • Stability Testing & Storage
  • Biostatistics & Statistical Programming
  • Data Management & eClinical
  • Regulatory Affairs
  • Medical Writing
  • Computational & In-Silico Drug Discovery
  • Translational Research
  • Target Identification & Validation
  • High-Throughput Screening
  • Medicinal Chemistry
  • In Vitro Pharmacology
  • In Vitro ADME / DMPK
  • Safety Pharmacology
  • Genetic Toxicology
  • Discovery Research
  • In Vivo Efficacy Models
  • In Vivo PK / PD Studies
  • GLP Toxicology
  • Preclinical In Vitro Studies
  • Preclinical In Vivo Studies
  • Bioanalysis
  • LC-MS Bioanalysis (Small Molecule)
  • Ligand-Binding Bioanalysis (Large Molecule)
  • Phase I Clinical Trials
  • Biomarker Assays
  • Phase II Clinical Trials
  • Phase III Clinical Trials
  • Clinical Operations
  • Phase IV / Post-Marketing
  • US FDA Regulatory Strategy
  • US FDA Regulatory Strategy
  • EU EMA Regulatory Strategy
  • EU EMA Regulatory Strategy
  • Japan PMDA Regulatory Strategy
  • Japan PMDA Regulatory Strategy
  • China NMPA Regulatory Strategy
  • China NMPA Regulatory Strategy
  • Clinical Trial Services
Modalities
  • Small Molecule
  • Biologics (Other)
  • Cell Therapy
  • Gene Therapy
  • Small Molecule
  • Small Molecule
  • Biologics (Monoclonal Antibodies)
  • Biologics (Monoclonal Antibodies)
  • Biologics (Other)
  • Biologics (Other)
  • Peptide
  • Peptide
  • Oligonucleotide
  • Oligonucleotide
  • mRNA
  • mRNA
  • Antibody-Drug Conjugate (ADC)
  • Antibody-Drug Conjugate (ADC)
  • Gene Therapy
  • Gene Therapy
  • Cell Therapy
  • Cell Therapy
  • Vaccine
  • Vaccine
Indications
  • Cardiovascular
  • Dermatology
  • Gastroenterology
  • Immunology
  • Infectious Disease
  • Metabolic
  • Neurology
  • Oncology
  • Ophthalmology
  • Psychiatry
  • Respiratory
  • Women's Health
  • Oncology
  • Rare Disease
  • Immunology
  • Immunology
  • Neurology
  • Neurology
  • Psychiatry
  • Metabolic
  • Metabolic
  • Cardiovascular
  • Cardiovascular
  • Infectious Disease
  • Infectious Disease
  • Respiratory
  • Respiratory
  • Dermatology
  • Dermatology
  • Ophthalmology
  • Ophthalmology
  • Gastroenterology
  • Gastroenterology
  • Nephrology
  • Nephrology
  • Women's Health
  • Women's Health
Locations
  • Headquarters, Montreal, Quebec, Canada
  • Bioanalytical Laboratory, Laval, Quebec, Canada
  • Clinical Site, Montreal, Quebec, Canada
  • Clinical and Research Campus, Overland Park, Kansas, United States
  • Preclinical Testing, Everett, Washington, United States
  • Manufacturing and Analytical Services, Harleysville, Pennsylvania, United States
  • Preclinical Testing, Scranton, Pennsylvania, United States
  • Preclinical Testing, Columbia, Missouri, United States
  • Clinical Pharmacology, Cypress, California, United States
  • Preclinical Testing, Sacramento, California, United States
  • Laval, Laval, Quebec, Canada
  • Overland Park, Overland Park, Kansas, United States
  • Everett, Everett, Washington, United States
  • Harleysville, Harleysville, Pennsylvania, United States
  • Cypress, Cypress, California, United States
  • Scott Township, Scott Township, Pennsylvania, United States
  • Auxvasse, Auxvasse, Missouri, United States
  • Sacramento, Sacramento, California, United States
  • Canada, Canada, Canada
  • United States, United States, United States
  • Canada and U.S. operations
  • Global network
  • Global presence, 30 countries
  • Global presence, Multiple, 30 countries, Global
  • Global presence, Multiple, 30+ countries
  • Global presence, Multiple, 30 countries, International
  • Headquarters, Radnor, Pennsylvania, United States
  • Global presence, 30 countries
  • Global presence, 30+ countries
Certifications
  • FDA · Identifier: FDA inspection passed 2001
  • GLP · Identifier: GLP Compliant
  • GMP · Identifier: GMP Manufacturing
Data not yet provided.
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.