ClinTech Research is a service company focused on preclinical development, founded in 2005 as a New Jersey, USA company with a subsidiary in India.

The Leadership Team of ClinTech Research is led by Sri P Srivastava, PhD, Founder & CEO who has technical experience related to the full range of pharmaceutical R&D activities. Furthermore, he has substantial project management experience in the pharmaceutical industry in the USA.

The focus of ClinTech Research is on Integrated preclinical drug development also draws on practical awareness of drug discovery & clinical development meaning that Dr. Srivastava is uniquely qualified to operate as general manager of this process for client companies.

The principle of integration is addressed by large pharmaceutical companies in-house but CROs do not usually focus on this need. In contrast, ClinTech Research is an independent integrating CRO that provides an opportunity for biotechnology companies to achieve large pharmaceutical industry standards.

In addition, it is important to recognize the parallel priorities of Time, Cost, and Reliability that clients require. ClinTech Research believes that it is ideally placed to meet this need since the practical work is done globally by a network of appropriate CRO sites in the USA and offshore… With regards to offshore sites India is considered to be particularly important because of long standing historical awareness of FDA regulatory requirements, reasonable cost and the wide range of CRO contacts in that country aided by the Indian office of ClinTech Research.

Our Advantage:

ClinTech Research's goal is to provide a high quality of service using our US/India hybrid model. We work hand-in-hand with you to manage your projects; and offer the following advantages as your offshore partner:

• US/India hybrid model providing offshore advantage with US expertise.
• Single point-of-contact liaison/ technical project management in the USA
• Partners network infrastructure in place.
• FDA 21 CFR Part 11 and System Validation experience within the US Industry.
• Data center in the USA with advanced physical and information security.
• Access to Regulatory & QA advisors/consultants in the USA and India.