Clinical Operation

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The very first step always creates difficulties.
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