::: Clintox Bioservices :::

Our primary goal at Clintox is to help our sponsors succeed in a competitive marketplace.

As an offshore testing service partner, Clintox offers a distinct strategic advantage for its sponsors!

Clintox is committed to helping our sponsors get the most of their R&D by providing preclinical services that shall be GLP Compliant and High Resource Efficient.


	Clintox understands the criticality of preclinical trials to the R&D plans of its sponsors.

	Clintox ensures full accountability at all times to its sponsors.

	How? Clintox empowers its clients with the unique ability to control and monitor the off-site preclinical studies from remote locations.

	We have implemented Toxchek, a state-of-the-art preclinical LIMS that helps us conduct our toxicology studies in a protocol driven environment in compliance with USFDA and WHO requirements.

	Further, sponsors shall be provided with unique usernames using which they can access our trials database - through this, sponsors can not only monitor but also control the progress of their trials.

Quality:
Clintox conducts toxicology studies in compliance with the norms prescribed by OECD and ICH. SOPs are designed and strictly adhered to in order to ensure quality compliance.

Clintox has already initiated the process of GLP certification by OECD and also AAALAC certification.