::: 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:
All toxicology studies conducted at Clintox are GLP compliant as per OECD guidelines. Our Quality Assurance Unit conducts a thorough audit at every step of study planning and execution from protocol preparation till draft and final report preparation. Our QAU shall issue a GLP Compliance Statement for every study conducted at our facility.