Site Management

SMS (Beijing) ClinicalStudies Co., Ltd. is one of the earliest and most professional SMO companies in China and a professional service institution assisting clinical trial institutions in on-site management and specific operation. As a leading SMO company in China, SMS is committed to providing professional and efficient SMO services, assisting research institutions and investigators in the management of clinical trials, improving the quality and progress of clinical trials and promoting the standardized process of clinical trials.

SMS has on-site management business at clinical sites in more than 100 cities across the country, has a stable professional team of about 1,000 people, has established international standard operating procedures, provides professional services for more than 500 sites across the country, has won extensive praise from investigators, and has become a preferred supplier for many institutions. SMS has operational experience in more than 800 clinical research projects in oncology, BE & phase 1, cardiovascular, hematology, endocrinology, neuropathy, respiration, dermatology, gynecology, gastroenterology, psychosis, vaccines, and medical devices.

Comprehensive and accurate data are included in a mature project management system, which can provide strong support for customers such as site screening and project progress estimation, and guide project managers to accurately control project progress, identify project risks as soon as possible, and take effective measures to ensure project quality. After many years of development, SMS has become a long-term partner of a number of well-known domestic and foreign pharmaceutical enterprises.

Relying on the professional clinical site management team, systematic business training and good relationship with the sites and investigators, SMS provides professional and efficient clinical study services with a scientific, rigorous and pragmatic attitude.

Services include:

Rapid initiation, subject management;

Ethics submissions and follow-up, patient referral and in-hospital recruitment;

Document management, data acquisition and entry;

Coordinate with local laboratory, monitor on-site filing support;

Trial vendor management, investigational product management;

Site closure, third party audit services.