English (United States)

CIEC organized “GOOD CLINICAL PRACTICE Professional courses”

reduce font Size enlarge font Size print content

CIEC organized “GOOD CLINICAL PRACTICE Professional courses”

For new investigators: “Introduction to Good Clinical Practice” held on 10th March 2018 at CHL by Sophie Moya Quality Assurance Manager Development, Medical & Regulatory Affairs (Cefira trainer)


For experienced investigators: “Modern Risk Management in Clinical Trials” held on 13th June 2018 at CHL by Ingrid Klingmann, MD, PhD Chairman, European Forum for Good Clinical Practice (EFGCP)

This GCP annual session has been held with success! The advanced Training for Experienced Investigators and Research Teams has reached a total of 53 participants with 32 external attendees.

30 participants attended the basic session with 20 attendees outside LIH.

Many topics have been discussed such as:

• An Update on GCP requirements for investigators under the ICH-GCP new version E6R2
• How to handle risks in a clinical trial?
• Relevance of the Informed Consent Process for minimisation of the risk of low patient recruitment and retention
• How to improve the Informed Consent Process at the site?
• Essential tools in clinical trial organisation
• How to better organise the clinical trial at my site?



Who should register?

Healthcare professionals who wish to be part of a unique network, providing access to up-to-date, accurate and validated information about clinical research.

Investigators and study staff who wish to be part of a unique network, in order to stay abreast of clinical trials taking place in Luxembourg and who are willing to further develop their competencies.