Our Experience
To date there have been more than 400 clinical trials conducted at TTMC’s sites in the past ten years. Among them, 90% are global trials, 95% are multi-center projects, and about half are early phase (II and IIIa) studies for NDA submission purpose. Our clients include international pharmaceutical companies, contracted research organizations (CROs), medical device companies, and biotechnology companies.
Clients
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SMO Services
Feasibility
- Delegated staffs for professional feasibility study in multiple sites
- Site and PI recommendation
- Consultation for site/investigator selection
- Database Survey
- PI interview
- Trustworthy feasibility report
Site Coordination
- Provide/Organize training & education programs for site staff
- Establish and coordinate investigator team
- Establish infra-structure for trials in hospitals
- One-stop service for internal & external parties in a site
- One-stop service for multiple sites within the network
Trial Conducting
- Provide dedicated, full-time and experienced Clinical Research Coordinators on-site
- Assist in visits and meetings arrangement & FU
- Assist in accelerating the processof IRB if possible
- Set up central recruitment campaign for trials
- Assist in the preparation and conduct of monitoring, audit and inspection
A good SMO would benefit
Sites
- Investigators and Sites need assistance
- Well-established infra-structure & well-trained, dedicated staff are essential for quality trial conduct and performance
- Good performance bring income and reputation to sites
Sponsor
- Efficient and accurate feasibility response
- Efficient contract process for multiple sites
- Efficient pre-study preparation
- Efficient subject recruitment
- Good compliance and high quality of conduct
- High retention rate for trial subjects
- Efficient query resolution
Patients
- In good hands
- 24 hours, 7 days a week, professional care