Study Management and Monitoring
Our partners can assist your organization with managing and monitoring your clinical studies worldwide. We can assist your organization with IRB/EC/REB Regulatory Submissions, Study Plans including Data Management, Monitoring, Safety, Site Selection, Qualification, and Initiation, Vendor Selection and Management, Contract and Budget Negotiations, Site Training and Management, Data Management, Trial Branding, Investigator Meetings, Site Training, Case Support, Clinical Trial Document Authorship, Publication Authorship and Publication Assistance, and Trial Rescue Services. We can also customize your monitoring strategy based on your study needs. Our monitoring services include clinical trial monitoring, risk-based monitoring, and remote monitoring.