Sponsors
Translational Clinical Research prides itself on our professional team’s experience and integrity.
A few examples of our experience includes:
- First in Human
- Bio-Equivalence
- Broncho-Provocation Challenge Testing
- Drug – Drug Interactions
- Food Effect
- Phase I Oncology
- Nutriceuticals
Translational Clinical Research is known for our ability to complete technically and logistically demanding protocols. Our success is based on our precision in sample collection (Pharmaco-Kinetic, Pharmaco-Dynamic and Biomarker samples), along with sample processing requiring complex methodologies. We strive for zero deviations.
Our large computerized database consists of normal healthy, elderly, HTN, diabetic, asthmatic, surgically sterilized, and post menopausal women volunteers. We also have access to other specialty populations through local advertising and community physician referrals.
Our Central IRB has four Boards and conducts up to thirteen convened Board meetings a week. All ICFs and patient information material is IRB approved in both English and Spanish, in order to accommodate our population. We want to accept the challenge of your most technically demanding studies to be completed with the safety and well being of the participants, while adhering to proposed study timelines. We are timely in locking clinical databases. Our eCRF (EDC) data entry has < .01% error rate. Please give us the opportunity to work with you and take your compounds from “Bench to Bedside”. Our experienced clinical team makes us the best CRO for technically demanding studies.
Our Clinical Research staff has completed more than 100 Phase1 and over 200 Phase 2-4 trials. Professional journal publications, co-authored by our team’s investigators, can be provided upon request. For more information please call us at 305.705.3623 (main professional line) or email us at Sponsors@TranslationalCR.com
