Intox is as an experienced GLP complaint preclinical testing partner with over 25 years of experience in conducting safety assessment studies. From designing a complete study program to running every single test, Intox can address all your requirements. Safety Assessment studies are performed in compliance with global regulatory guidelines such as ICH, FDA, EMA, EU, OECD, OPPTS, JMAFF, CIB. We work in a collaborative manner, using our expertise to accomplish the safety assessment of your product. Toxicology testing defines the hazards from product exposure and plays a critical role in ensuring the safety of humans, animals and environment.
Rely on our toxicology testing capabilities when it comes to acute/single dose and repeat dose study designs (subacute/chronic). Our expert team enables the shortest turnaround time for study completion to expedite regulatory submissions. They can implement all dose routes including dietary, oral gavage, dermal, inhalation and parenteral in all laboratory animals viz., rats, mice, rabbits, Guinea pig, hamster, dog and NHP. All animal experiments are reviewed and approved by the Institutional Animal Ethics Committee (IAEC). Our 50-room animal facility is approved by the CPCSEA, Government of India, and meets global standards of maintenance and operation as prescribed by CPCSEA. Historical data accumulated over the years is available on in-life parameters, clinical and anatomic pathology, genetic toxicology and DART studies.
Acute Six pack / Single Dose toxicity
Repeat Dose Studies in rodents and non-rodents
Developmental and Reproductive Toxicology
Special Toxicology (single/repeat dose)
