Questra’s team has a combined experienced of over 35 years in clinical trials handling sites resources, project management, data management and statistical analysis. Our team’s sites experience and knowledge has equipped us with insights crucial to the success of clinical trials, an added value that is built in our clinical trial management.
Clinical trial sites with high standards of investigator quality, at competitive cost and assurance of fast patient recruitment.
To meet your expectations and walk the extra mile in delivering our services to you with integrity, quality & timeliness, ethically and within budget.
Services for Bioavailability / Bioequivalence studies with assurance of standards of compliance, good practices, and quality processes.