Home|Submit RFP|Contact Us|
  • Company
    • About
    • History / Leadership
    • Corporate Values / Mission
    • News
    • Events
    • Corporate Presentation
  • Locations
    • US
    • China
  • Services
    • Preclinical
      • Preclinical Overview
      • GLP Toxicology Studies
      • In Vitro ADME Studies
      • In Vitro Metabolism & Identification
      • Pharmacokinetic Studies
      • Safety Pharmacology
      • Scientific & Regulatory Affairs Consultation
    • Bioanalytical
      • Bioanalytical Overview
      • LC/MS/MS & GC/MS Method Development / Validation
      • Clinical Biomarker & Immunogenicity Services
      • Biomarker Assay Development / Validation
      • Pharmacokinetic / Pharmacodynamic Modeling
      • Streamlined Sample Management & Processing
      • Scientific & Regulatory Affairs Consultation
    • CMC Services
      • CMC Services Overview
      • GMP Analytical Services
      • Finished Product Development
      • GMP Manufacturing - Clinical Trial Materials
      • GMP API Manufacturing & Organic Synthesis
      • ICH Stability Storage & Testing
      • Unknown Impurities Identification Projects
      • Scientific & Regulatory Affairs Consultation
    • Clinical Research
      • Clinical Research Overview
      • Phase I-IIa Facilities
      • Pharmacokinetic (PK) Evaluations
      • Data Management
      • Statistical Analyses
      • Medical Writing
      • Patient Recruitment
      • Regulatory Consulting Services
  • Careers
    • Opportunities
    • General Resume Submission
  • Study Participation
    • Current Studies
    • Facilities
    • FAQs
    • Enroll In A Study
    • Directions to Clinic
  • Scientific Showcase
    • Assay List
    • Publications and Case Studies

Site Map

Home

Submit RFP

Contact Us

 

  • Company
    • About
    • History/Leadership
    • Corporate Values/Mission
    • News
    • Events
  • Locations
    • US
    • China
  • Services
    • Preclinical
      • Overview
      • GLP Toxicology Studies
      • In Vitro ADME Studies
      • In Vitro Metabolism & Identification
      • Pharmacokinetic Studies
      • Safety Pharmacology
      • Scientific & Regulatory Affairs Consultation
    • Bioanalytical
      • Overview
      • LC/MS/MS & GC/MS Method Development/Validation
      • Clinical Biomarker & Immunogenicity Services
      • Biomarker Assay Development/Validation
      • Pharmacokinetic/Pharmacodynamic Modeling
      • Streamlined Sample Management & Processing
      • Scientific & Regulatory Affairs Consultation
    • CMC Services
      • Overview
      • GMP Analytical Services
      • Finished Product Development
      • GMP Manufacturing - Clinical Trial Materials
      • GMP API Manufacturing & Organic Synthesis
      • ICH Stability Storage & Testing
      • Unknown Impurities Identification Projects
      • Scientific & Regulatory Affairs Consultation
    • Clinical Research
      • Overview
      • Phase I-IIa Facilities
      • Pharmacokinetic (PK) Evaluations
      • Data Management
      • Statistical Analyses
      • Medical Writing
      • Patient Recruitment
      • Regulatory Consulting Services
  • Careers
    • US Opportunities
    • China Opportunities
    • Submit Resume
  • Study Participation
    • Enroll In A Study
    • FAQs
    • Current Studies
    • Facilities
  • Scientific Showcase
    • Assay List
    • Case Studies

1. Footer Navigation

HOME | COMPANY | LOCATIONS | SERVICES | CAREERS | STUDY PARTICIPATION
SCIENTIFIC SHOWCASE | FRONTAGE CHINA | SITE MAP | CONTACT US

224 Valley Creek Blvd, Suite 300, Exton, PA 19341
TEL 610.232.0100 | FAX 610.232.0101

© 2010 Frontage Laboratories, LLC

Site design by SCORR Marketing