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Monitoring

Well-conducted monitoring adds undeniable value to any clinical study. Besides overseeing the progress of a clinical trial, monitoring protects trial participants and ensures data integrity. This key quality control activity is critical for adhering to good clinical practice (GCP). We offer expertise and up-to-date practical tools for monitors so they can set up well-conducted monitoring even when their budget is tight.

Effective guardians of processes and people in clinical studies

What we offer:

We provide monitors with expertise and practical tools to efficiently conduct the monitoring of a clinical study. These tools can be tailored to single-centre or multicentre studies in Switzerland and beyond.

What challenges we tackle:

Resources for investigator-driven clinical studies (IICT) and other clinical studies initiated in an academic setting are often limited. We help with solutions that can be carried out even when the budget is tight, for example by supporting you with the implementation of a risk-based monitoring approach in line with the requirements of GCP.

Our key projects:

We develop tools for implementing a risk-based strategy for the monitoring of clinical trials, such as a risk-score calculator and its accompanying Guideline for Risk-Based Monitoring (as provided in the SCTO’s Guidelines for Good Operational Practice (GGOP)).

Furthermore, we harmonise the monitoring processes for Swiss multicentre, investigator-initiated studies (IICT), for example by providing a template for a monitoring plan and templates for monitoring visit reports and a template for the site initiation visit.

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The minds behind the Monitoring Platform

We are experts from all over Switzerland who channel our efforts to provide up-to-date resources for well-conducted monitoring within academic clinical research, from single-centre to complex multicentre studies. We aim to effectively harmonise monitoring documentation and offer our expertise across language barriers.

Coordinator

Dr Jocelyne Chabert
Geneva University Hospitals (HUG)
CRC Geneva

Team

Jocelyne Chabert, CRC Geneva, Coordinator

Jocelyne Chabert, CRC Geneva, Coordinator

Klaus Ehrlich, DKF Basel

Klaus Ehrlich, DKF Basel

Yves Franzosi, CTU-EOC Lugano

Yves Franzosi, CTU-EOC Lugano

Sandra Handgraaf, CRC Geneva

Sandra Handgraaf, CRC Geneva

Christina Huf, SCTO

Christina Huf, SCTO

Simone Kälin, CTU St.Gallen

Simone Kälin, CTU St.Gallen

Sara Mantero, CRC Lausanne

Sara Mantero, CRC Lausanne

Sophie Mermoud, CTU Bern

Sophie Mermoud, CTU Bern

Luzia Steiner, SAKK

Luzia Steiner, SAKK

Markus Vaas, CTC Zürich

Markus Vaas, CTC Zürich

Martina Zimmermann, CTU Bern

Martina Zimmermann, CTU Bern

Our tools and resources

Get in touch with us

We are your primary contact point for monitoring activities in the field of clinical research in Switzerland. To receive competent answers to general monitoring questions, contact us at or use the form below.