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From Study Concept to Regulatory Success
Our services are designed to bridge the gap between research execution and strategic decision-making. We partner with you to ensure your programs meet the highest standards of scientific rigor, regulatory compliance, and operational efficiency.
Research Strategy & Design
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Study concept development
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Protocol creation and refinement
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Statistical planning & analysis consultation
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Data governance and integrity frameworks​ from the start to ensure scientific, operational, and regulatory success
Extensive international experience
Triligent has delivered outstanding results to clients in more than fifty countries
A well established operation producing outstanding results as evidence by a high rate of repeat business
Diverse Subject Matter Expertise
Oncology
Infectious Disease
Nephrology
Gastroenterology
Organ Transplant
HIV/AIDS
Immunology
Cardiology
Neurology
Pediatrics
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How is a RCO Different from a CRO?
In the life sciences, CROs (Contract Research Organizations) deliver operational execution — running trials, monitoring sites, and managing data collection.
As a Research Consulting Organization (RCO), Triligent operates differently. We focus on:
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Strategic Study Design — aligning protocols with both regulatory pathways and scientific goals
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Independent Oversight — ensuring compliance, data integrity, and operational efficiency across all vendors and sites
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Regulatory & Quality Assurance Guidance — preparing your program for inspections, submissions, and investor review
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We complement CRO activities, rather than replace them — ensuring your research is built on a foundation of rigor, transparency, and strategic foresight.
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