Our objective is to provide you with ethical, quality oriented, enthusiastic, and experienced clinical research sites in an efficient manner. We can help speed up the site identification, qualification, initiation, budget/contractual negotiations and start up process. Our internal management and operating procedures are specifically designed to quickly provide you with multiple and highly qualified sites that meet your specific criteria. Because we only present those sites that meet your self-defined needs, you can significantly reduce the time and resources required to evaluate and qualify a site or Principal Investigator.

We provide the Sponsors/CRO, the following services:

• Pre Study Planning & Feasibility
• Investigator Identification
• Site Evaluation & Site Set up
• Clinical Trial Management
• Study Team Training
• Trained Clinical Research Professionals who can deliver effective site coordination and trial management
• Streamlined Project Management
• Customized Patient Database
• Customized Patient Recruiting Strategies
• Timely and Accurate Data Entry, Safety Reporting and Query Resolution
• Centralized Feasibility, Contract Development & Budgeting, Project Management for sites, Clinical  
   Relations and Quality Control
• Strategic Relationship Building with site staff and synchronized working patterns for each site
• Periodic Mentoring and Quality Checks of each site

Faster CTA Negotiations
Successful Patient Enrollment Results
Higher patient retention
State-of-the-art Facilities
Full-time Trained and Experienced Staff
Clinfound Clinical Research Services Pvt. Ltd.
3/160 A, VKV lane,
Chembumukku, Kakkanad West PO,
Kochi, Kerala-682 030
Mob: +91 999 534 2978