Advanced Good Clinical Practice Training – Informed Consent Today : Requirements, Options and Opportunities
04/06/2019 13:30 to 04/06/2019 17:30 (Europe/Luxembourg)
Luxembourg,
Luxembourg
The Clinical and Epidemiological Investigation Center is organizing an advanced Good Clinical Practice Training. The training is highly recommended to all persons involved in research projects with human participants.
The training will be held in English.
PROGRAMME
13:30 | Welcome and introduction
13:40 | Informed Consent process under the upcoming Clinical Trial Regulation
14:15 | Informed Consent under the GDPR
14:30 |The MHRA recommendations for eConsent
14:50 | Joint discussion: How to optimise the Informed Consent process in patients able to consent
15:15 | Break
15:45 | Joint discussion: How to optimise the Informed Consent process in vulnerable patients
16:15 | Exercise: How to plan the Informed Consent process
17:00 | What did I learn? Final Multiple Choice Test
17:30 | End of training
SPEAKER
Ingrid Klingmann
MD, PhD Chairman, European Forum for Good Clinical Practice (EFGCP)
Language: English
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: Tuesday: 4th of June 2019
Where: Centre Hospitalier Luxembourg (CHL)
Amphithéâtre
4, rue Barblé
L-1210 Luxembourg
Time: 1:30 p.m. – 5:30 p.m.
Contact: tania.zamboni@lih.lu
