Services offered to Sponsors & CROs

Our Customized Recruitment Campaigns and specialized clinical facilities gain success from utilizing the following strategies:

Pre-Study

  • Study Specific Site Selection and On Site Facility Assessment
  • IRB Document Preparations and Submission
  • Regulatory Document Preparation and Submission
  • Budget Negotiation and Preparation
  • CTA Review
  • Site specific SOPs provided
  • Qualified Research Staff provided
  • Staff GCP Training
  • Source Document Templates
  • Multicenter queries are managed through centralized communication by highly a qualified project manager.

Study Conduct

  • Site Initiation Visit preparation
  • Timely review of CRFs and all documents
  • Quality Assurance
  • Attendance at Monitor Visits, Documentation, and Resolution of queries
  • Ensure ICH/GCP Compliance
  • Provide Staff Training
  • Participant Recruitment services
  • Monitoring and Independent Audits (QA)

Post-Study

  • Study Close-Out
  • Query Resolution
  • Study Material archived for 25 years
  • Site Follow-Up