what we DO

Areas of Expertise

We combine our expertise, experience and innovation  in order to achieve the high quality service with  clinical research professionals for the success of the research project.
Bioequivalence
We support all aspects of generic drug development, from sample size calculation and design issues at the planning stage, to analyzing, displaying and interpreting data in the final stages of the study.
Food Supplements
Food Supplements Clinical Trials can be an essential component for substantiating health claims for foods and food constituents and supplements. We offer Institutional Review Board for review and approval of clinical trial designs in case trials are not a subject to Regulatory Agency approval and Central Ethics Commitee Approvals
Cannabinoids
Small scale preliminary in house studies conducted in order to evaluate feasibility, time, cost, adverse events, and effect size (statistical variability). Our team are experts in cannabinoid products design, production set up and clinical testing.
Phase I/II
Our wide array of therapeutic expertise enables us to address the most demanding drug development challenges. We collaborate with you to develop a better future for patients by bringing our expertise to clinical development through the commitment of our employees.
Cosmetics Products
We help to ensure the safety and efficacy of your cosmetics and consumer healthcare products through in house clinical testing.
Pilot
Small scale preliminary studies conducted in order to evaluate feasibility, time, cost, adverse events, and effect size (statistical variability) in an attempt to predict an appropriate sample size and improve upon the study design prior to performance of a full-scale research project.
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