ICRS offers professional services for CROs, private research practices, and other research organizations.  Those services include creating the Essential Documents for trial conduct, audit, and inspections. Our specialists at ICRS are expert in creating the following documents:  

• Informed Consent Forms (ICF’s)
• Subject Logs
• Participant Information Sheets
• Source Documents
• Case Report Forms (CRF’s)
• Screening, Enrollment Logs
• Recruitment, Randomization Logs
• Study document
• Serious Adverse Event Form/Safety Report
• IRB submission Tracking Log
• Investigational Product Accountability Log
• Patient-Reported Outcomes Forms (PRO)
• Specimen Tracking Log
• Delegation of Authority Log
• Other