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WELCOME TO PACIFIC BIOLABS: HOMEPAGE

• CONTACT US
  • Map and Directions
• ABOUT PBL
  • Why Work With PBL
  • Mission and Quality Policy
  • Quality Systems
    • PBL Testing Process
    • Continuous Improvement
    • Testing Regulatory Decision Tree
    • ISO Certification
    • cGMP/GLP Compliance
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    • SOP Manual
    • Archive Policy
  • Facility
  • History
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• TESTING SERVICES
• In Vivo Toxicology
• Pharmacokinetics / Radiolabeled ADME
• Custom Studies
• Cytotoxicity
• Stability Testing
• Safety Tests
• Bioassays
• Harmonized Microbial Limits Test
• Antimicrobial Effectiveness and Time Kill
• Pharmaceutical Sterility Testing
• Pharmaceutical LAL, Endotoxin and Pyrogen Testing
• Bacterial Identification
• Pharm/Biopharm Environmental Monitoring
• USP Water Testing
• Biocompatibility Testing
• USP Class Plastics Testing
• Device Shelf-Life / Accelerated Aging
• Device Endotoxin Testing
• Device Sterility Testing
• Device Sterilization Validations
• Cleaning and Disinfection Validations
• Contact Lens Solution Testing
• Package and Container Tests
• Textile Antibacterial Activity Assessment (AATCC)
• EPA / OPPTS Testing
• LEARNING CENTER
  • Pharmaceutical and Biotech Development
    • Drug Development Process
      • Stages of Drug Development
      • Drug Development Process: Critical Steps
      • Timeline of Studies
      • Outsourcing Strategies
      • Planning Outsourced Testing
    • In Vivo Testing Overview
    • Categories of Preclinical Studies
      • Exploratory Studies
      • Regulatory Studies
      • Formulation Support
      • Microdosing
      • Downloadable Test Timing Chart
    • Regulations
    • Animal Welfare / IACUC
    • References
  • Pharmaceutical and Biotech Quality Control
    • Compendial Bioassays
    • Compendial Microbiology
    • Toxin Testing
    • Microbiology/Sterility Testing
    • Water Testing
  • Medical Device
    • Assessing Biocompatibility
      • Intro to Biocompatibility Testing
      • Test Planning (BioPT)
      • Biological Test Methods
      • Analytical Testing of Biomaterials
    • USP Class Plastics
    • Sterilization Validations
      • Validation Planning
      • Radiation Sterilization
      • Ethylene Oxide Sterilization
      • Steam Sterilization
      • Chemical Sterilization
      • Sterilization Validations: References
    • Sterility Assurance Tests
    • Reusable Device Validation Studies
      • Webinar
• CONSULTING SERVICES
• RESOURCES FOR CLIENTS
  • Quotation Request Form
  • LSR forms
  • LSR Submission Checklist
  • Service Terms and Conditions
  • Client Feedback Form
  • Technical Links
• BLOG
• SUBMIT SAMPLES
• PRIVACY POLICY
• TEST STATUS REQUEST FORM