CRP is international company which was established by clinical research professionals in 2015. Our mission is to develop clinical trials infrastructure in Russia and EU and provide a range of unique services: 1. Site Management Organization: The company in cooperation with few medical institutions established a network of dedicated investigator sites conducting phase I-IV clinical trials under the "Clinical Research Partner" quality standards. Also SMO provides support to partner Investigators in other sites. The key advantages of working with our network are good data and documents quality, quick subjects' enrollment and commitment to timeliness. The network includes dedicated fully equipped and managed by "Clinical Research Partner" sites located in Russia (St.-Petersburg, Saratov) and Bulgaria (Sofia) Each network site has all required staff, equipment and facilities to conduct a study. Some medical centers have own local laboratory and radiology facilities. All investigator sites work according to unified standards (SMO Quality Management system). 2. Network Independent Ethic Committee provides ethic coverage for all sites. IEC could also provide ethic coverage for other sites which don't have own LEC. 3. Educational program on the base of clinical trial training center which provides a set of different training (Pharmacoviligance, GCP, coordinator and etc) and Quality Management services For feasibility questions please contact us via email info@crptrials.com www.crptrials.com
