Clinical Trial Management
Improving the health and safety of patients is our mission at Clynico Consulting. We work with your team to ensure that clinical trials conducted at your sites follow study protocols and local/international regulations.We provide various services to clients ranging from independent medical office to established sponsor/CRO:
- Source Document Review
- Source Document Verification
- Adverse Event Monitoring
- Study Initiation Documentation/Meetings
- Study Monitoring (Including Interim Inspection Visits)
- Regulatory Compliance (Patient Consent forms, Staffing logs, HIPPA, Standard Operating Procedure material)
- Staff training
- Site/Patient Recruitment
