At VxP Pharma, a complete range of toxicological services are available to support the dermal administration route in multiple animal models, pre-clinical studies and/or clinical trials.
Our toxicology team can provide extensive expertise with both large and small molecule drug candidates targeting a wide range of therapeutic areas. Specialized tox services are also available to meet your development needs for specific bioanalytical/TK research or safety studies. With multiple qualified toxicologists, we can support all stages of the drug development process in accordance with current Good Lab Practice (GLP) guidelines.
- Acute Dermal Toxicity
- Acute dermal irritation/ corrosion
- Repeated dose dermal Toxicology
- Ocular Toxicology
- Dermal Toxicity at Injection site
VxP Pharma offers rapid and dependable (GLP and Non-GLP) toxicokinetic analyses, interpretation and TK reporting of bioanalytical data generated from preclinical toxicology and drug metabolism studies. Our TK reports are specifically designed to meet client-specific formats, and will be comprehensively reviewed by our full service Quality Assurance Department.
Related TK Services
- Acute / Sub-chronic / Chronic Toxicology
- Dose Range Finding (DRF)
- Development & Reproductive Toxicology (DART)
- Dermal Toxicology
- Ocular/Ophthalmic Toxicology
- Pathology / Clinical Pathology
Our preclinical team has extensive experience working with the FDA, USDA, and EPA required to make your animal research projects a success. Specifically tailored, individual study designs enable our clients to meet their product development goals and facilitate regulatory approval. Our individualized approach to each study allows us to revise and shift directions based on your timeline and/or changing needs.
Our state-of-the-art labs are staffed by some of the best trained and most experienced subject matter experts in the field.