What We Do

Clinical trials are the “Gold Standard” for product claim support, differentiation, sales and marketing. Standards conducted its first published clinical trial in 1999 and since that time, has worked to streamline/standardize the process for affordability. It designs and authors protocols for Institutional Review Board (IRB) submission/approval and International Standard Randomised Controlled Trials Number (ISRCTN) registration. On study completion, Standards compiles the data, writes the paper and submits it to an appropriate open-access journal for review and publication. Working with academic institutions and medical schools in Mexico and Central and South America, cost are typically one-third that of a similar trial conducted in the United States or European Union.