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Clinical Trial Management System

. . . for Sites engaged in Phases 1, 2, 3 & 4 of clinical trials

Are You ...

	Juggling with multiple excel files & papers to figure out how your study is progressing?
	Finding it hard to keep track of where your subjects are in your studies?
	Bogged down with sorting appointment clashes?
	Worried about missing those important lab reports?
	Having too many staff handling very few studies?

If your answer to the above questions is a YES, we have the solution for you. All the above concerns, and many more, are addressed in our CTMS

How CTMS for Sites helps in conducting clinical trials?

Our Clinical Trial Management System is a work flow oriented operations management software for sites that conduct clinical trials. Designed by Principal Investigators & Study Coordinators with years of experience in conducting clinical trials, our CTMS is focused to help you conveniently and efficiently manage all activities entailing your site's day-to-day operations.

	Conveniently manage various types of studies - regular, multi-arm, observational & extensions. Create your own study process flow.
	Increase the number and size of trials your organization manages with fewer additional resources. No need to spend exponentially to grow exponentially.
	CTMS consolidates and streamlines protocol visits scheduling, allocation of staff & equipment resources, subject tracking, site and staff document tracking, financial tracking, site monitoring, and more. Provides full site workflow management from study start-up to closeout, allowing you to manage more and larger trials with less resources/overhead and eliminate protocol violations.
	A comprehensive process driven system enables your staff to focus less on the administrative tasks and more on direct patient care.