Consistent, coded, and compliant.
Aquila MS ensures that safety and clinical data are standardized, traceable, and ready for regulatory submission, including regulatory classification mapping such as MedDRA and WHO ATC.
Smart data connections for transparent reporting.
Aquila MS API solutions such as Aquila Scope bridge systems and processes through standardized data mapping and API-based integration.
Precision in documentation, clarity in compliance.
Regulatory data management and submission oversight for sponsor and study support functions.
▪ EMA Sponsor & SPOR registration and maintenance
▪ XEVMPD (Article 57) data submissions
▪ CTIS setup, QC, and update coordination
▪ Document lifecycle management
Strategic support for compliant and efficient safety operations.
Aquila MS provides specialized consulting across pharmacovigilance systems, quality management, and operational oversight — from process design to document maintenance.
PV system setup, maintenance & procedural documentation Safety data workflow optimization and SOP alignment Cross-functional PV training and continuous improvement support