Non-Clinical (GLP) Testing Services
Ensuring Safety and Compliance from the Ground Up
Our Non-Clinical (GLP) Testing Services are designed to support your drug development process by ensuring that all safety and toxicology studies comply with Good Laboratory Practice (GLP) standards, as required by regulatory agencies like the U.S. FDA and EU MDR.
Our services include:
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Safety and Toxicology Studies: Conducting comprehensive safety assessments, including acute, sub-chronic, and chronic toxicity studies to ensure your product’s safety profile.
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Pharmacokinetics and Pharmacodynamics (PK/PD): Detailed studies to understand the absorption, distribution, metabolism, and excretion (ADME) properties of your compound, along with its pharmacological effects.
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Carcinogenicity Studies: Long-term studies to evaluate the potential cancer-causing effects of your drug candidates, in compliance with GLP standards.
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Genotoxicity and Reproductive Toxicity: Assessing the genetic and reproductive safety of your compounds to ensure they meet regulatory requirements.
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Environmental Risk Assessment: Evaluating the potential impact of your products on the environment, a key requirement for regulatory submissions.
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Comprehensive Reporting: Providing detailed, GLP-compliant reports that are ready for submission to regulatory agencies, ensuring your data is both reliable and credible.
By partnering with us for your non-clinical GLP testing needs, you can be confident that your product is safe and ready for the next stages of development.