Ensuring data integrity and analytical confidence in dissolution testing

Ensuring data integrity in pharmaceutical dissolution testing, where results inform both product release and stability assessment, is vital as labs shift to digital workflows. Manual records and disconnected systems pose compliance risks and limit traceability.

Discover how ERWEKA DT 950 / 9510 software v3.0 solves these challenges with embedded audit trails and role-based access, supporting scientists to meet regulatory standards with confidence and efficiency.