The Duopharm team will help you organize and conduct early-stage and bioequivalence clinical trials, as well as provide consulting support for late-stage clinical trials. By entrusting the Clinical Trials to DuoPharm professionals, you are guaranteed to get:
- clear regulated work in cooperation with regulatory authorities
- timely recruitment of the required number of research centers
- high speed of recruitment of clinical trial subjects
- proper quality of all procedures and regulations
- strict compliance with current Russian and international legislation
- access to information about the progress of research
We will help you set up processes for organizing clinical trials in both large research centers and small institutions with complex logistics chains. In accordance to your request DuoPharm will evaluate the feasibility of conducting clinical trials in Russia before the start of the study. We’ll help you form a “third” opinion for making an informed and right decision in the beginning of your project.