Frontage Laboratories
Integrated drug discovery and development services across 28 global sites.
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Global pharmaceutical development organization offering integrated drug discovery, preclinical safety/toxicology, DMPK, bioanalytical, and clinical trial services across 28 sites with 2,200 employees and 200+ FDA inspections.
Phases
Indications / Therapeutic Areas
Services
- Medicinal Chemistry
- Computational & In-Silico Drug Discovery
- In Vitro ADME / DMPK
- In Vitro Pharmacology
- Preclinical In Vitro Studies
- Safety Pharmacology
- Genetic Toxicology
- DART (Reproductive & Developmental Toxicology)
- GLP Toxicology
- In Vivo PK / PD Studies
- In Vivo Efficacy Models
- Preclinical In Vivo Studies
- Phase I Clinical Trials
- Phase II Clinical Trials
- Clinical Operations
- Bioanalysis
- LC-MS Bioanalysis (Small Molecule)
- Ligand-Binding Bioanalysis (Large Molecule)
- Immunogenicity Assays (ADA / NAb)
- Biomarker Assays
- Flow Cytometry Services
- Central Laboratory Services
- Pathology & Histology Services
- Genomics & Sequencing Services
- Biostatistics & Statistical Programming
- Data Management & eClinical
- Medical Writing
- Analytical Method Development & Validation
- ICH Stability Studies
- Discovery Research
- Target Identification & Validation
- High-Throughput Screening
- Specialized & Large-Animal Models
- Phase III Clinical Trials
- Clinical Trial Services
- Regulatory Affairs
- US FDA Regulatory Strategy
Modalities
Technical specifications & accreditations
Accreditations
Infrastructure
About this organization
Overview
Frontage Laboratories is a global pharmaceutical development organization (PDO) advancing drug discovery and development through integrated laboratory and clinical services. The company operates 28 sites across North America, Asia-Pacific, and Europe with approximately 2,200 employees worldwide.
Service Offerings
Drug Discovery
- Frontage Global Drug Discovery Service (GDDS) provides end-to-end drug discovery services
- Chemistry and biology capabilities
- ADME/Tox screening
- Pharmacology services
- Medicinal chemistry
- Target identification and high-throughput screening
- Permeability and transporter studies
- Protein binding and physicochemical properties assessment
- Metabolite identification
Drug Development
- DMPK (Drug Metabolism & Pharmacokinetics) services
- In vitro services
- In vivo services including PK/TK studies and QWBA studies
- Preclinical Safety & Toxicology
- General toxicology
- Specialized toxicology services
- Developmental and reproductive toxicology (DART)
- Global pathology services
- Early-phase clinical services
- Biometrics
- Biostatistics
- Medical writing
Laboratory Testing Services
- Bioanalytical services
- Small molecule modalities
- Antibody-drug conjugate (ADC) analysis
- PK/TK studies
- Assay development
- Central laboratory services
- Clinical trial support
- Biospecimen and data services
- Biorepository services
- History and pathology
- Safety testing and specialty lab testing
- Central lab e-portal
CMC & Product Development
- Chemistry, Manufacturing and Controls services
- Analytical services for small molecules
Agrochemical Support
- GLP-compliant facility support for agrochemical clients
- Biological, chemical, and regulatory support
Regulatory & Compliance
The organization has undergone 200+ FDA inspections, demonstrating extensive regulatory engagement and compliance experience.
Certifications
| Authority | Identifier | Source |
|---|---|---|
| FDA | 200+ FDA Inspections | View |
Locations
Headquarters
Global Operations
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