GLP Toxicology Studies

To assess toxicity, Medicilon offers a wide range of GLP and non-GLP toxicology services. GLP and non-GLP Toxicology studies are required to determine the adverse effects of drug candidates and the effect of dosage on toxicity.

Preclinical CRO / Toxicology Studies Include:

Late-Stage Discovery Studies

• Pharmacokinetics Study (PK)

• Maximum Tolerated Dose Studies (MTD)

• Dose Range Finding Study

• hERG – Ion Channel Screening

• Exploratory Toxicology Study (7-day non-GLP Studies with PK)

GLP Toxicology Studies

• 7-day Repeat Dose Study (GLP)

• 14-day Repeat Dose Study (GLP)

• 21-day Repeat Dose Study (GLP)

•   3-month Chronic Repeat Dose Study (GLP)

• 6-month Chronic Repeat Dose Study (GLP)

• 9-month Chronic Repeat Dose Study (GLP)

• Carcinogenicity Studies (Transgenic & 2 year)

Safety Pharmacology Studies (GLP)

• Cardiovascular Study (Telemetry or Piggy-backed)

• Respiratory Study

• Central Nervous System Study (CNS Study)

Genetic Toxicology (Genetox)

• Ames Assay (non-GLP & GLP) CRO

• Micronucleus Assay

• Chromosomal Aberration Assay

With extensive experience in drug development, Medicilon staff is dedicated to helping you complete your project in a timely and efficient manner. In addition to Good Laboratory Practice (GLP) toxicology studies, Medicilon provides all aspects of the GLP process from design to regulatory support of your IND FDA submission. Our preclinical team has extensive experience in set-up and management of GLP animal toxicology studies and other experience across all facets of preclinical research, from identification, assessment and due diligence on new compounds to conduct of animal models.

Contact Us

Email : marketing@medicilon.com

Tel : +86 021 5859-1500

Tips : Above is part of GLP Toxicology Studies, GLP Toxicology and Toxicology Testing Labs. You can also CONTACT US with any question or enquiry you may have. We will be happy to discuss your needs in detail and design an appropriate plan of action.

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