QVIS

QVIS provides comprehensive SOP development services according to sponsor-specific requirements, ICH-GCP, and European and U.S. clinical trial directives and regulations.
SOP development areas are listed below and can be prepared in Korean or English.

· Clinical trial-related activities including clinical operations
· Quality management activities for clinical trials
· Pharmacovigilance-related activities

QVIS also performs gap analysis by reviewing existing SOPs and supports revisions accordingly.
SOP development includes the development of forms required for SOP implementation.