Preclinical Drug Development and Research | Pharma Product Development Services
Your Partner in Pharmaceutical and Biopharmaceutical Product Development
At Toxikon, we understand how important on-time delivery is for meeting your goals for IND, NDA, and other international submission requirements. That’s why we approach your pharmaceutical development needs— from efficacy, safety to analytical studies— using a very systematic approach. This allows us to apply our extensive knowledge, experience and diverse capabilities. As your development partner, we work side-by-side with you to learn the intricacies of your application, and deliver timely reports with results you can use and depend on.
Toxikon’s full breadth of preclinical pharmaceutical services includes:
- Pharmacology, PK/TK
- Reproductive Toxicology
- Flow Cytometry
A Practical Approach to Preclinical Development
While our reputation has been built on our vast toxicology experience, Toxikon’s scientific experts know how to navigate the regulatory landscape during the development of both large and small molecules. It starts with proof of concept and progresses through pharmacokinetics, toxicokinetics, formulation development, and a full range of analytical and bioanalytical services. Toxikon has the ability to use a wide variety of small and large animal models, including mice, rats, guinea pigs, rabbits, dogs, cats, hamsters, goats, swine, and non-human primates. Our facilities include surgical suites with special imaging and analysis capabilities for all specialized and/or custom programs.
We understand just how critical development support is from concept through essential safety and efficacy studies. At Toxikon, our approach involves three main values. First, we are committed to quality and scientific excellence. Second, our client-centric, collaborative approach will give you confidence knowing that our scientists understand your application, and third, the know-how to navigate the regulatory landscape for your product’s development path. With Toxikon, you get more than a highly qualified CRO, you get a partner, who understands and has the experience to design, validate and execute all preclinical study requirements.
The Development Path