Together with our partners, SynRG offers scientific support throughout study lifecycle. To this end SynRG provides the following services:

Medical Writing

• Development, review and finalization of study protocol and investigator brochures
• Development of clinical study reports
• Development of patient informed consent forms
• Development of summary documents

Data Management

• CRF / Diary Design
• Edit Checks
• Lab Uploads
• SAE Reconciliation
• AE Coding
• Med Coding
• Medical History Coding
• Interim Database Lock
• Data Transfers

Biostatistics

• Study Design Support
• Statistical Analysis Plan
• Design of Table Shells (Mocks)
• Programming/QC of Data Displays
• Statistical Analysis
• Interim Analysis
• Statistical Report
• Interim Statistical Report
• Data Transfers