Good Laboratory Practices

Ensuring study data is generated and reported with quality and integrity

Corner Bubbles

Supporting Good Laboratory Practices (GLP) on a global scale
Quality assurance from our global network of suppliers

Since 2007, has been working across the industry to enable Faster Science. Quality is critical when you are conducting research, so our award-winning compliance platform, COMPLi®, puts important information at your fingertips to remove barriers and drive research pipelines forward.

COMPLi® enables users to access a customizable compliance process that complements internal strategies and provides visibility, transparency and control. Our request for information (RFI) pre-assessments allow suppliers to proactively share key information with researchers in an easily-digestible and structured manner, highlight their capabilities and increase their visibility. Easily review supplier responses to our GLP RFI, communicate approved suppliers to your entire research base and view key information during the supplier selection process.

Embedded functionality across various categories

Execute to GLP standards and confidently source studies



    In Vivo

    Anatomic Pathology
    Dose Method Development and Validation


    Analytical Development and Validation
    Formulation Development
    Stability Testing

Your GLP research is in good hands
Feel confident in speeding up research while improving compliance

With instant access to hundreds of global suppliers across many disciplines, researchers are able to quickly find what they need, and quality teams can ensure only approved suppliers are accessed. Whether you are working towards your first regulatory submission or your 30th, COMPLi® enables an organization to access a bespoke compliance process that complements internal strategies and provides visibility, transparency and control. Researchers no longer need to contact suppliers to access information required to elect the best supplier for their research — as this information is already available at their fingertips. is proud to also offer concierge and category expert teams, composed of PhD scientists who are available to aid in the sourcing process 24/7. Our strong industry presence further enables us to support researchers in other service categories, including ensuring efficient access to suppliers conducting your research under GLP conditions.

Hundreds of services available, including:


  • Anatomic Pathology
  • Histopathology
  • Bioanalysis Method Development and Validation

Chemistry, Manufacturing and Controls (CMC):

  • Analytical Development and Validation
  • Formulation Development
  • Stability Testing

In Vivo:

  • OECD 487: In Vitro Mammalian Cell Micronucleus Test
  • Repeat Dose Intravenous Infusion Study
  • OECD 432: In Vitro 3T3 NRU Phototoxicity Test
  • Topical Dermal Toxicity and/or Toxicokinetic Study
  • OECD 473: In Vitro Mammalian Chromosomal Aberration Test
  • OECD 471: Bacterial Reverse Mutation Test
  • Enhanced Pre/Post-Natal Development Study
  • Carcinogenicity Study

Learn more about our category offerings:

In Vivo

Access in vivo services efficiently and compliantly

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Animal Welfare

Ensure animals in research are handled ethically and humanely

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Access hundreds of global chemistry services instantly

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Providing global access to biomarker services

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Improved sourcing of regulated scientific services

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Expand visibility to compliant providers to speed up research in a controlled and compliant manner

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