Dedicated coordinators
A GCP-trained CRC handles scheduling, documentation, data entry and sponsor communication under your supervision.
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For investigators and hospitalsRun high-quality research without stretching your team
You bring clinical expertise and patients. We bring trained coordinators, documentation and study management, so research fits around your practice.
Less paperwork for you
We prepare EC submissions, maintain the site file and keep logs current, so your time goes to patients and medical decisions.
Access to studies
We bring sponsor and CRO opportunities that match your specialty and patient population.
Pharmacy support
Pharmacist oversight of investigational product storage, dispensing and accountability.
Inspection readiness
SOP-driven conduct and regular internal QC, so monitoring visits and audits run smoothly.
Training for your team
GCP and protocol training for sub-investigators and site staff, with records maintained.
How a partnership starts
Simple, transparent and on your terms
We start with a conversation about your department’s interests, capacity and infrastructure. There is no cost to be added to our investigator network, and you choose which studies to take on.
Join our investigator networkIntroductory meeting
We learn about your specialty, patient volume and research experience.
Site profile
We document infrastructure, staff and EC arrangements, once, so feasibility requests move quickly.
Study matching
We bring suitable studies and handle feasibility with your input.
Start a conversation
Planning a study in India?
Share your protocol synopsis and target indication. We will come back with a site feasibility view within five working days.