Avacare SMO Service_KUNTUO

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Avacare
The Trusted Choice of SMO Site Management Services
About Avacare
Avacare’s Clinical Research Coordinator (CRC) team has provided CRC services successfully in over 1000 clinical study projects for more than 900 sites since the team was built up, highly appreciated by sponsors, investigators and other cooperating CROs (responsible for project management and monitoring). No serious or major issue has been found yet during every audit and quality control. Our performance has been highly trusted and fully appreciated by sponsors and institutions. Our excellent performance on various projects during the review by National Medical Products Administration (NMPA) and US FDA has facilitated successful market launch for a range of products.
Highly Qualified Team and Efficient Management Processes
Highly Qualified Team and Efficient Management Processes
Our CRC management team is highly experienced in clinical trials and has a proven track record in management of clinical trial sites, part of which previously worked in the clinical operation department in the multinational pharmaceutical companies; therefore, they completely understand sponsor needs.
We own a highly qualified CRC team. All team members majored in nursing, medicine, pharmacy or other related disciplines, being familiar with the working procedures and environment of hospitals as well as the work and communication styles of the investigator teams.

100%100%

of the team members majored in nursing, medicine, pharmacy and other related disciplines

85%85%

of the team members got Bachelor or the above education degree

5.4years+5.4years+

of work experience on average

3.5years+3.5years+

of clinical trial experience
Avacare Services
Why Choose Avacare?
Abundant Resources of Sites and Investigator Data
Abundant Resources of Sites and Investigator Data

Cost-effective - Avacare is able to provide high-quality services at local prices. In each major therapeutic area, we are keeping close contact with the sites and the academic leaders, so as to provide you with wide and professional medical support and expert counseling in strategy establishment and protocol design, ensuring a reasonable and effective study strategy and protocol.
Our team owns the resources of clinical study sites and the investigator database in China shared by IQVIA which includes thousands of high-quality investigator information and site information, supporting Avacare to identify sites quicker and recruit subjects faster. As a result, the study initiation can be accelerated, so as to save time and resource costs for clients.

Wide-ranging Business Areas
Wide-ranging Business Areas

Extensive Service Coverage
Extensive Service Coverage

Avacare’s CRC services are available in over 50 cities, including capital cities and the second tier and third tier cities of China where lots of clinical studies are located
The work efficiency of CRC can be extremely increased to minimize the costs of the project operation for clients

Flexible and Feasible CRC Services
Flexible and Feasible CRC Services

The completed SOP systems are perfectly applicable to clinical studies in China
Huge clinical study database
Flexible service based on customer needs

Abundant Resources of Sites and Investigator Data

Wide-ranging Business Areas

Extensive Service Coverage

Flexible and Feasible CRC Services

Full-covered Therapeutic Areas
Customize Your Clinical Study Protocol