Clinical Trial Monitoring In-house Training

This course will assure monitors understand the importance of compliance with latest ICH GCP R3 requirements, and how these apply to monitoring clinical trials in the future.

★★★★★ "Fantastic, energetic, and positive. Very clear describing of the topics and good structure. Discussi... more"

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Format: Bespoke training
CPD: 12 hours for your records (depending on your requirements)
Certificate of completion

Course overview

With regulatory inspectors increasingly finding GCP issues with monitoring clinical trials, it is becoming even more important for the biopharmaceutical industry, study sites, and CROs to employ efficient and accurate strategies for monitoring clinical trials. Also, the global COVID-19 pandemic has changed the ways clinical trials are monitored and resulted in remote and centralized monitoring techniques at the forefront of monitoring. This has created an environment that requires monitors to not only purely focus on site visits. Regulatory authorities promote these alternative ways of monitoring trial data and the future is likely to include a more hybrid monitoring approach.

This highly interactive course, which includes group discussions, ensures that monitors not only understand the importance of compliance with the latest GCP standards but also gain insights into how new monitoring approaches are shaping the future of clinical trials.

Browse our extensive selection of Life Sciences training courses for industry-leading insights into a range of topics. These include Medical Devices, IVDs, Biotech and Biopharma, Animal Health and Pharmaceutical training courses.

Benefits of attending

Ensure GCP compliance for monitoring clinical trials including during Covid and monitoring approaches for the future
Evaluate the development of monitoring plans through protocol analysis for remote risk management
Discuss tools and risk evaluation approaches for remote monitoring
Ensure appropriate site selection, initiation, monitoring, and close out visits are carried out including during a pandemic
Review sponsor and CRO oversight of monitors

Who should attend?

Monitors
Clinical research associates (CRA)
Clinical trial managers
Study coordinators
Project managers
Research nurses
Study site assistants
Those responsible for oversight of monitoring
Investigators seeking to move into clinical trial monitoring

This course will benefit those involved in the monitoring of clinical trials, including new and soon-to-be monitors. This will also be an ideal refresher including how monitoring has changed because of the pandemic and those responsible for oversight of monitors.

Reviews of IPI's Clinical Trial Monitoring training course

Fantastic, energetic, and positive. Very clear describing of the topics and good structure. Discussions. It made me feel more involved in the webinar.

Jul 29 2024

Viktoriia Kyrylenko Ukraine
Project Manager, BIOPHARMA PLASMA LLC