WEBINAR: How to plan and perform clinical trials during and after the COVID-19 pandemic (LIH-EFGCP GCP Refresher Training)
02/06/2021 13:00 to 02/06/2021 17:30 (Europe/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.
PROGRAM
13:00 | Introduction
13:10 | History of changes in clinical trial conditions during the pandemic
13:30 | Requirements and options for adaptation of study conditions during the pandemic respecting EMA and diverse national guidances on different trial aspects, e.g.,
Informed consent
IMP handling
Decentralisation of study activities
Protocol deviations
Pharmacovigilance
Monitoring
Auditing and Inspections
Communication with ethics committees and competent authorities
15:00 | Break
15:30 | Lessons learned: How to plan a clinical trial that will start in September 2021?
16:20 | Joint Exercise: Risk Management in a clinical trial in times of a pandemic
17:00 | Final multiple-choice test
17:30 | End of the Training
TRAINER
Ingrid Klingmann
MD, PhD, FFPM, FBCPM, GFMD
Expert in Medicines Development Planning and Site Management Support
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 |
Organized by Clinical and Epidemiological Investigation Center in collaboration with:
