State-of-the-Art Clinical Facility

Dedicated exam and procedure rooms, secure, temperature-controlled IP storage, 24/7 environmental monitoring systems, on-site laboratory capabilities to streamline sample handling and processing.

Regulatory

We operate in full compliance with FDA, GCP, and IRB regulations, with internal SOPs and QA oversight to ensure integrity at every stage of the trial.

Integrated Data Managment & E-source Systems

Our fully integrated electronic source (eSource) systems allow for:

   – Real-time patient data entry and monitoring

   – Efficient patient identification and prescreening

   – Reduces query turnaround times and remote sponsor access

Experienced, Multi-Disciplinary Research Team

Our team brings over 25 years of experience in Phases II-IV clinical trials, including:

   – Board Certified Principal Investigators with extensive clinical and research backgrounds

   – Certified Clinical Research Coordinators proficient in GCP, recruitment, and data integrity

   – Regulatory and Quality Assurance personnel dedicated to compliance and documentation accuracy

Dedicated to Delivering Reliable Data & Efficient Study Execution

Clintex Research Group is dedicated to fast site activation, accurate data collection, and streamlined operations. We pride ourselves on being responsive, adaptable, and committed to delivering on timelines without compromising quality.