Training - Good Clinical Practice (for Confirmed Investigators) - EN
13/06/2018 15:00 to 13/06/2018 19:00 (Europe/Luxembourg)
Luxembourg,
Luxembourg
Luxembourg,
Luxembourg
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 |
Registration
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 |
Information
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
Contact:tania.zamboni@lih.lu