Monitoring

Professional clinical monitoring for maximum data quality and GCP compliance.

Our qualified clinical monitoring team ensures the integrity of your study data and compliance with Good Clinical Practice (GCP) through risk-based monitoring strategies.

Thanks to our many years of experience in oncology and multicenter clinical trials, we support trial centers and investigators in successfully conducting their trials.

Range of clinical monitoring services

On-site and remote monitoring of clinical trials
Risk assessments and development of study-specific monitoring plans
Selection and evaluation of suitable study centers
Initiation visits including initial training of study personnel on the protocol
Ongoing support of study centers and continuous communication to ensure data quality and patient safety
Closing visits for structured study termination

Luzia Steiner

Head of Monitoring & Clinical Project Management

+41 31 508 41 59 luzia.steiner@swisscancerinstitute.ch