Triumpharma houses a fully GLP-compliant bioanalytical facility with state-of-the-art infrastructure managed by qualified and expert staff with experience in more than 150 different drug development and analysis
Triumpharma clinical site is a state of the art research facility dedicated for clinical research (bioequivalence, Phase I) . Our clients are relying on our site to consistently meet or exceed enrolment goals and capture accurate, high quality data while maintaining superior standards of care in accordance with FDA regulations and ICH/GCP guidelines.
The clinical sites include drug and specimen storage area, equipped for PK sampling and emergency unit. The clinical site possesses ample space to comfortably accommodate subjects during routine and extended visits and offer secure record storage on site.