Altasciences vs Syngene International

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Category	Altasciences	Syngene International
Listed site	both	both
Summary	Mid-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.	Innovation-led CRDMO offering integrated scientific services from early discovery through commercial manufacturing, with cGMP-compliant facilities, 5,200+ scientists, and a new 50,000-liter single-use bioreactor capacity in the U.S.
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	Discovery Research Medicinal Chemistry Computational & In-Silico Drug Discovery In Vitro Pharmacology In Vitro ADME / DMPK Safety Pharmacology GLP Toxicology Analytical Method Development & Validation Formulation Development Process Development CMC Analytical Development Small Molecule Development & Manufacturing API Synthesis & Manufacturing Sterile Fill-Finish & Aseptic Manufacturing Vial Filling Prefilled Syringe (PFS) Filling Cell-Line Development Recombinant Protein Manufacturing Monoclonal Antibody (mAb) Manufacturing Biologics Development & Manufacturing Upstream Processing Downstream Processing Bioanalysis Peptide Manufacturing Oligonucleotide Manufacturing ADC (Antibody-Drug Conjugate) Manufacturing Cell Therapy Manufacturing mRNA Manufacturing Translational Research High-Throughput Screening Genetic Toxicology Preclinical In Vitro Studies Preclinical In Vivo Studies In Vivo Efficacy Models In Vivo PK / PD Studies Carcinogenicity Studies DART (Reproductive & Developmental Toxicology) Specialized & Large-Animal Models LC-MS Bioanalysis (Small Molecule) Ligand-Binding Bioanalysis (Large Molecule) Immunogenicity Assays (ADA / NAb) Biomarker Assays Flow Cytometry Services Clinical Trial Services Phase I Clinical Trials Phase II Clinical Trials Phase III Clinical Trials Phase IV / Post-Marketing Clinical Operations Data Management & eClinical Biostatistics & Statistical Programming Pharmacovigilance & Drug Safety Medical Writing Central Laboratory Services Clinical Imaging Core Lab Regulatory Affairs US FDA Regulatory Strategy EU EMA Regulatory Strategy Japan PMDA Regulatory Strategy China NMPA Regulatory Strategy ICH Stability Studies Companion Diagnostics Development Microbiology Services Virology Services Immunology & Inflammation Services Oncology Specialty Services CNS Specialty Services Cardiovascular & Metabolic Specialty Services Pathology & Histology Services Genomics & Sequencing Services Proteomics Services Bioinformatics & Data Science Device & Combination Product Services HPAPI Manufacturing (High-Potency) Controlled Substance Manufacturing Flow Chemistry & Continuous Manufacturing Solid-State Chemistry & Polymorph Screening Microbial Fermentation ADC Payload & Linker Synthesis Bioconjugation Services Viral Vector Manufacturing AAV Manufacturing Lentiviral Vector Manufacturing Autologous Cell Therapy Manufacturing Allogeneic Cell Therapy Manufacturing Lipid Nanoparticle (LNP) Formulation Vaccine Manufacturing Microbiome / Live Biotherapeutic Manufacturing Cartridge Filling Lyophilization (Freeze Drying) Oral Solid Dosage Manufacturing Topical & Semi-Solid Manufacturing Inhalation & Nasal Dosage Manufacturing Ophthalmic Manufacturing Technology Transfer Quality Control Testing Stability Testing & Storage Extractables & Leachables Studies Secondary Packaging & Labeling Serialization & Track-and-Trace
Modalities	Small Molecule Biologics (Other) Cell Therapy Gene Therapy	Small Molecule Biologics (Monoclonal Antibodies) Biologics (Other) Peptide Oligonucleotide Antibody-Drug Conjugate (ADC) Cell Therapy mRNA Gene Therapy Vaccine
Indications	Cardiovascular Dermatology Gastroenterology Immunology Infectious Disease Metabolic Neurology Oncology Ophthalmology Psychiatry Respiratory Women's Health	Rare Disease Oncology Immunology Neurology Psychiatry Metabolic Cardiovascular Infectious Disease Respiratory Dermatology Ophthalmology Gastroenterology Nephrology 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	Headquarters, Bangalore, Karnataka, India U.S. Biologics Facility, United States U.S. Biologics Facility, San Diego, California, United States
Certifications	FDA · Identifier: FDA inspection passed 2001 GLP · Identifier: GLP Compliant GMP · Identifier: GMP Manufacturing	Data not yet provided.
Reviews	Review summary appears after site-level review signal gate opens.	Review summary appears after site-level review signal gate opens.