Biocard Research offers a range of clinical and business services designed to make the process of conducting a clinical trial (from the study design development and feasibility analysis to the study close out) in Russia as seamless and cost-effective as possible. We can provide a comprehensive range of services on the organization and conduct of clinical trials:
• Medical Writing including IB, clinical study protocol, ICF, CRF and final report on the clinical study results;
• Feasibility analysis and selection of investigational sites;
• Regulatory services including study documents preparation and submission;
• Clinical trial management;
• Clinical monitoring;
• Logistics management (via "Biocard Logistics");
• Customs clearance (via "Biocard Logistics");
• Study drug and materials storage and distribution (via "Biocard Logistics");
• Laboratory samples export (via "Biocard Logistics");
• Central lab and analytical lab selection and management;
• Data management;
• Statistical analysis;
• Translation.
Our experience and reach throughout Russia comes in many forms. A wealth of region-specific knowledge, contacts, infrastructure and resources can add significant value to a new study. Our approach is strictly focused on optimizing the region’s potential to bring new compounds to market with greater efficiency and cost effectiveness, and ultimately meet and exceed increasingly demanding study goals.
With a sharp business focus and an unyielding commitment to deliver world-class quality and service, we provide sponsors with the comprehensive support required to successfully conduct and complete a clinical trial. Throughout the process we put an emphasis on being both responsive and flexible to changing needs.