Indago Research and Health Center is a fully integrated clinical research site with the capacity to conduct Phase I/II through IV clinical trials supported by a 44,000 sq ft facility, advanced diagnostics, and a multidisciplinary operational model with access to a database of over 40,000 volunteers.
Our infrastructure, technology ecosystem, and specialized departments enable complete end-to-end study execution that includes feasibility assessment, regulatory start-up, recruitment, clinical operations, sample handling,
data accuracy, and compliant close-out.
The site’s capacity, resources, and personnel qualifications meet the operational standards required by FDA, GCP, and ICH guidelines.
Indago has successfully completed more than 400+ clinical trials in both acute and chronic conditions in the following areas:

Immunologic and respiratory-focused studies.

Hypertension, lipid management, and cardiovascular outcome trials.

Topical and systemic treatments for chronic skin conditions.

Infection, inflammation, and respiratory system disorders.

Diabetes, obesity, and hormonal metabolism trials.

Multicondition general practice protocols.

Functional and inflammatory gastrointestinal disorders.

Post-surgical recovery and pain management protocols.

Kidney function, chronic renal insufficiency, and metabolic research.

Migraine, cognition, and neurodegenerative disorder studies.

Weight management and dietary supplement studies.

Visual acuity and ocular disease studies.

Depression, anxiety, and cognitive therapy protocols.

Asthma, COPD, and respiratory infection trials.

Arthritis, inflammation, and autoimmune disease research.

Sleep apnea and circadian rhythm studies.

Urinary tract and male reproductive health trials.

Adult and pediatric preventive vaccine studies.

Conditions focused on women’s biology, hormonal balance, menopause, and reproductive health.

Clinical research studies focused on children’s health and development.
Indago’s operations are supported by specialized facilities, certified laboratory and pharmacy units, and advanced diagnostic equipment that ensure data precision, patient safety, and regulatory compliance.
With modern equipment, proper environmental controls for sample integrity, robust IT systems for data security, and flexible spaces that can accommodate different protocol requirements, Indago serves as a trusted research partner for sponsors and CROs worldwide.

Indago’s facility is fully equipped with advanced medical and diagnostic tools. All instruments are maintained, calibrated, and documented according to GCP and FDA audit readiness standards.












Data integrity and security. Real-time visibility. Operational efficiency.
Indago integrates a fully connected digital ecosystem that ensures operational traceability, secure data flow, and efficient multi-department communication, giving sponsors real-time confidence in site performance without requiring continuous oversight.
All platforms are maintained by the internal IT Department, which manages hardware, software, user access, network security, and system integrations in full alignment with FDA, GCP, and HIPAA requirements.
The department also partners with specialized cybersecurity providers for 24/7 monitoring, penetration testing, and routine system audits, reinforcing complete data protection and operational reliability.

Top Technology Benefits
Advanced cybersecurity framework: providing sponsors with peace of mind through 24/7 monitoring.
eISF (Electronic Investigator Site File)
Manages all regulatory documentation, training logs, delegation records, and IRB correspondence.
Real Time Devana (CRM)
Tracks study feasibility, contracts, sponsor communication, and performance metrics, providing visibility across business development and clinical teams.
SharePoint / OneDrive
Provide secure document sharing, SOP management, and version control across departments.
RealTime ePay
Secure digital payment system used to compensate study participants promptly and confidentially, ensuring accuracy, transparency, and full compliance with FDA and financial audit standards.
To see our operations in person, contact us for a site visit or take a virtual tour of our facility.
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