SibPharma provides quality service to spnsors by understanding the specific needs of the client and adapting to those needs. SibPharma brings a broad scope of expirience to a project including legal information and Internet technology, as well as investigators and associates from a range of therapeutic areas. Its experienced, highly qualified staff and the international setup through the Russian-German partnership enables SibPharma to quickly identify and adapt to the needs of a project. SibPharma strictly observes GCP, the requirements of regulatory evironment, and the fundamentals of professional project management.

Active quality assurance reduces monitoring time and minimizes data queries. Project managers are respnsive to the needs of sites and CROs.

SibPharma services include:

• Selection of qualified top recruiting study sites
• Preparation of investigator meetings and site initiation
• Training site personnel
• Training and implementation of SOP
• Implementing a quality assurance program for accurate and timely collection of patient data
• Surveillance of the clinical trial process
• Assuriance of FDA/GCP guidelines & site monitoring