Welcome to SIBPharma

SibPharma is a Site Management Organization (SMO) that was founded as a Russian-German joined venture with its headquarter in Omsk, Russia. SibPharma delivers clincal trials research management services to pharmaceutical and biotechnology companies by providing marketing, administrative and patient recruitment services of clinical research sites and clinical investigators. To allow sponsors access to various sites and to link with highly focused investigators in a broad range of therapeutic areas, SibPharma operates an extensive partner network with major hospitals in Siberia. The company is able to support clinical trial processes (Phase I-IV trials) including GCP compliance and adherence to local and international regulatory guidelines, investigatror/staff training, providing experienced site personnel and implementation of successful patient recruitment and retention techniques.

While maintaining attention to each client’s corporate goals, SibPharma offers development solutions tailored to an individual product’s unique scientific, medical, and regulatory requirements. The record of trial operations performed by its Management highlights SibPharma’s ability to build and maintain a professional level of communication, to ensure a high level of accountability and to facilitate high demands sponsors have towards investigative sites.

SibPharma is committed to quality-assured trial outcomes accelerating pre-study site/PI responses, budget/contract agreements, Institutional Review Board (IRB) and Regulatory Authorities (RA) approval, study initiation and immediate pre-screening, all via our centralized management. Our focus is on vigilant patient safety and attaining stated sponsor study objectives. SibPharma’s associated clinics physicians and other supportive staff are well trained and committed to maintaining long term relationships and high ethical standards.