Training - Good Clinical Practice (for Confirmed Investigators) - EN

Registration for this event is now closed

The Clinical and Epidemiological Investigation Center is organizing a Good Clinical Practice training for Confirmed Investigators.

Modern Risk Management in Clinical Trials

15:00	Welcome and introduction
15:10	Update on GCP requirements for investigators under the ICH-GCP Addendum
15:30	Exercise and joint discussion: How to handle risks in a clinical trial
16:00	Relevance of the Informed Consent Process for minimisation of the risk of low patient recruitment and retention
16:15	Exercise and joint discussion: How to improve the Informed Consent Process at the site?
16:45	Break
17:00	Essential tools in clinical trial organisation
17:15	Exercise and joint discussion: How to better organise the clinical trial at my site?
17:45	Collection, assessment and reporting obligations for safety data from a site’s perspective
18:00	Exercise and joint discussion: How to improve safety data collection and assessment?
18:30	What did I learn? Final Multiple Choice Test
19:00	End of training

Odoo - Sample 2 for three columns

MD, PhD Chairman, European Forum for Good Clinical Practice (EFGCP)

Language: English

As the number of seats is limited, we will accept registrations on a first come first served basis.

		Fees
1st price category	LIH / IBBL Students / UNI / LCSB National hospitals national health care professionals researchers / PI national academia	€ 0
2nd price category	International academia	€ 100
3rd price category	Industry / private companies	€ 200

Organized by:

Clinical and Epidemiological Investigation Center

in collaboration with:

When: Wednesday 13 June 2018

Where: Centre Hospitalier Luxembourg (CHL)

Amphithéâtre
4, rue Barblé
L-1210 Luxembourg

Time: 3:00 p.m. – 7:00 p.m.

Followed by a cocktail