We design and deliver clinical trials with speed, precision, and compassion—helping sponsors meet milestones while giving participants access to cutting-edge care.
GCP-trained physicians and IATA-certified professionals
CLIA-certified labs with full temperature monitoring
Adherence to ICH E6 R2 and all regulatory requirements
Clinical Trials
We are a specialized site network running Phase I–IV clinical trials across leading therapeutic areas. Our hybrid model—on-site, in-home, and virtual—removes barriers for participants while giving sponsors predictable startup and reliable enrollment.
Patient-First Access: Flexible visit options, transportation, and multilingual navigators.
Data Without Compromise:Centralized QA, rapid query resolution, and standardized SOPs.
Speed With Discipline: Feasibility in 48 hours and site activation in ≤21 days.
Equity Made Measurable: Representation goals set and tracked at each site.
Rapid protocol fit reviews, single contracting, and centralized regulatory for faster study launches.
Multi-therapeutic sites, experienced PIs, and consistent SOPs ensure high-quality execution.
Omni-channel outreach, community partnerships, and patient navigators deliver faster enrollment and better diversity.
Home visits, telehealth, and eConsent tools make participation easier and adherence stronger.
Risk-based monitoring, in-house QA, and robust data management ensure clean data at lock.
We conduct trials across multiple high-impact specialties:
Hypertension, heart failure, lipid disorders
Diabetes, obesity, NASH
Rheumatoid arthritis, psoriasis, dermatology
Migraine, Alzheimer’s, cognitive disorders
Asthma, COPD, seasonal infections
Adult and pediatric vaccines, novel infectious agents
Diseases
Disorders
Metabolic Diseases
Diseases
Our facility is equipped with certified staff, advanced laboratories, and specialized equipment to support clinical trials effectively.
We stand apart through our commitment to excellence, patient-centric approach, and rigorous scientific standards.
Our core team includes MDs certified in Internal Medicine, Nephrology, and Clinical Research.
Full compliance with ICH E6 R2, GCP, and all regulatory requirements for flawless execution.
CLIA-certified labs, -70°C freezers, PBMC processing, and dedicated IP storage.
Dedicated exam rooms, infusion chairs, emergency response equipment
CLIA-certified labs, centrifuges, −20°C and −80°C freezers, PBMC processing, and IATA-trained staff.
Temperature-controlled storage with continuous monitoring, chain-of-custody logs, and audit-ready documentation.
eSource and EDC integration, digitized regulatory binders, and centralized QA oversight.
We maintain all essential documentation to ensure compliance and streamline study startup. Our centralized teams handle budgets, contracts, and regulatory requirements efficiently.
Full documentation acceptable to all major IRBs
All personnel GCP-trained and protocol-ready
Complete logs and documentation for inspections
Find answers to frequently asked questions about participating in clinical trials or partnering with Azul Bio Research for your study needs.
We conduct Phase II-IV clinical trials across multiple therapeutic areas including Internal Medicine/Gastroenterology, Mental Health, Nervous System Disorders, Endocrinology, Infectious Diseases, and Cardiovascular Diseases. Our focus is on providing high-quality data while ensuring participant safety and protocol adherence.
Participant safety is our top priority. We have board-certified physicians overseeing all trials, fully equipped emergency kits, and strict adherence to GCP guidelines. Our facilities include monitoring equipment and we maintain 24/7 temperature monitoring for all study medications. All staff are trained in safety protocols and adverse event reporting.
Our laboratories are CLIA-certified, and we have IATA-certified staff for proper specimen handling and shipping. All our physicians and research staff are GCP-trained, and we maintain compliance with ICH E6 R2 guidelines. We're also set up to work with central IRBs for efficient study approvals.
We have dedicated, isolated informed consent areas to ensure privacy. Our process involves a thorough explanation of the study by qualified staff, ample time for questions, and documentation that participants fully understand the trial before consenting. We use both paper and electronic consent forms as required by the protocol.
Our combination of board-certified physician leadership, certified research professionals, state-of-the-art facilities, and commitment to ethical research sets us apart. We offer centralized budget, contracts, and regulatory teams for efficient study startup, and maintain rigorous quality control throughout each trial. Our focus on both scientific excellence and participant care creates an ideal environment for reliable clinical research.
Mon - Fri: 8am to 5pm
Weekends: By appointment
Looking to accelerate your next study? Upload your synopsis for a 48-hour feasibility response.
(512) 731-0786
sjafri@AzulBioResearch.com
3531 Town Center Blvd., Suite 101, Sugar Land, TX 77479