Altasciences
Early phase CRO/CDMO moving molecules from preclinical through Phase II with integrated expertise and dedicated support.
Listed on cdmo.directory
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. Headquartered in Montreal, Canada.
Modalities
Development & manufacturing
Structured CDMO capabilities from verified public sources.
Manufacturing (M)
Regulatory clearances
Services
- Stability Testing & Storage
- Formulation Development
- In Vitro ADME / DMPK
- Phase IV / Post-Marketing
- Preclinical In Vitro Studies
- In Vivo PK / PD Studies
- Regulatory Affairs
- Clinical Operations
- Medical Writing
- Data Management & eClinical
- Biostatistics & Statistical Programming
- ICH Stability Studies
- Analytical Method Development & Validation
- Ligand-Binding Bioanalysis (Large Molecule)
- Bioanalysis
- Clinical Trial Services
- Phase II Clinical Trials
- Phase I Clinical Trials
- In Vitro Pharmacology
- Safety Pharmacology
- GLP Toxicology
- Preclinical In Vivo Studies
Indications
About this organization
Overview
Altasciences is a forward-thinking, mid-size early phase contract research organization operating in Canada and the U.S. The company offers biopharmaceutical companies of all sizes a proven, flexible approach to early drug development.
Services
CRO Services:
- Preclinical safety testing
- Clinical pharmacology (Phase I to Phase II)
- Bioanalysis (preclinical to Phase IV)
- Research services
- Ligand-binding bioanalysis
Integrated CRO/CDMO Capabilities:
- Formulation development for preclinical and clinical stages
- Pre-formulation investigations
- Formulation validations
- Stability assessments
- Compatibility testing
- GMP manufacturing
- Analytical services
- Lead candidate selection through clinical first-in-human (FIH) studies
Differentiation
Altasciences operates as a fully integrated CRO/CDMO with dedicated cross-functional teams and a proprietary scheduling system. The company emphasizes:
- Single point of contact ("Tell Us Once™" model)
- Centralized systems for transparency and data sharing
- 25–40% time savings through customized project plans
- 98% on-time delivery rate (2021)
- Seamless transition from preclinical formulation development to clinical trials
- Flexibility and service regardless of program size
- Efficient recruitment and study participant management
Certifications
Locations
Canada and U.S. operations
United States
United States · United States
Canada
Canada · Canada
Sacramento
Sacramento · California · United States
Auxvasse
Auxvasse · Missouri · United States
Scott Township
Scott Township · Pennsylvania · United States
Cypress
Cypress · California · United States
Harleysville
Harleysville · Pennsylvania · United States
Everett
Everett · Washington · United States
Overland Park
Overland Park · Kansas · United States
Laval
Laval · Quebec · Canada
Preclinical Testing
Sacramento · California · United States
Clinical Pharmacology
Cypress · California · United States
Preclinical Testing
Columbia · Missouri · United States
Preclinical Testing
Scranton · Pennsylvania · United States
Manufacturing and Analytical Services
Harleysville · Pennsylvania · United States
Preclinical Testing
Everett · Washington · United States
Clinical and Research Campus
Overland Park · Kansas · United States
Clinical Site
Montreal · Quebec · Canada
Bioanalytical Laboratory
Laval · Quebec · Canada
Headquarters
Montreal · Quebec · Canada
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