Clinical Operation
What you are looking for is already prepared here.
Start your valuable journey with our reliable team.
Our skilled and well-trained experts assure the high maturity level of study
outcomes and efficient interaction with sites. Based on clinical trial plan and
SOP, we keep the quality and accuracy of projects. From beginning to the end,
we’re ready to introduce you the whole route to get through this tough journey
with the appropriate sites and patients, developing strategies.
By close supervision following regulations, protocol and SOPs thoroughly, we
also minimize the risks caused by study delays and data quality issues. Going
through the multiple steps to next stage, we offer an experienced clinical
research professionals who took a specific and personalized training program
and maintain strong relationships with investigative sites to ensure successful
trial progress.
- Site Feasibility Study/Pre-Study Visit
- Study Initiation Visit
- Study Monitoring Visit
- Site Management
- Study Close-Out Visit
- Source Document Review
- Regulatory Document Review
- Investigational Product Accountability
- Report Generation
