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Tigermed has professional Site Management Organization (SMO) which provides customized on-site management and clinical operation services for study sites/investigators. Mainly focus on providing real-time assistance to investigators and sites non-medical judgment routine work of clinical trials, so as to ensure the accuracy and integrity of the study data, improve study performances and progress. It is dedicated to pushing forward the standardization and globalization of clinical trials in China.

SMO team had covered 48 cities across China, with over 250 full-time staffs until the end of 2014 and has set up international standard SOPs . With the background of nursing、medical、pharmacy and other professions, CRCs are not only attuned to ICH-GCP & China GCP and well trained by SOPs and other skills, but also experience with electronic data acquisition system, such as Inform, Data Track, Medidata Rave etc.


Service Scope
Services for Sponsor/CRO

Project Feasibility Study
IEC/IRB Submission
Investigator Meeting Organization
Subject Recruitment
Site Selection and Evaluation
Study Budget Management
Study-Specific Training
Internal Audit
Study Project Management
Study Drug and Supply Management

Services for Sites/Investigators
Study Management
Clinical Research Coordinator Placement
Site Binder Management
Subject Recruitment and Management
Study Supply Management
Data Management
Communication with Site/IEC
Study Information Management
Site Management
SOP Development for Sites
Site Certification Consulting
On Site Training for Site Staffs
Site Support During an Audit
Sit Support During SFDA Inspection
Study Budget Negotiation
Business Development And Promotion
Assist sites to look for new study opportunities
Assist sites to perform market expansion and business development