The revision of the ICH-GCP Guide entered into force on 14 June 2017. It maintains the original text from 1996, but adds definitions, clarifications on the existing text and, in particular, adds a comprehensive section on risk-based quality management responsibilities of the sponsor.
This training is intended for professionals working in clinical trials (investigators, clinical trial teams or referrals, ie clinicians, family doctors, study coordinators, study nurses), clinical research coordinators, clinical research organizations (CROs), members of ethics committees or competent authorities, researchers or other research staff.
The training curriculum complies with the minimum TransCelerated criteria of GCP training courses. Participants will have to pass a test to obtain the certificate of completion.
AVANTYO Institute of Clinical Research organizes these specialization courses
Ø Tuesday, August 25 | 10:00 - 17:15 Bucharest time (GMT + 3) https://avantyo.us3.list-manage.com/track/click?u=ab12985f2d6310c488c608ea1&id=6e8b9ce461&e=0df19a944a
Ø Tuesday, September 29 | 10:00 - 17:15 Bucharest time (GMT + 3) https://avantyo.us3.list-manage.com/track/click?u=ab12985f2d6310c488c608ea1&id=fe1eedd96d&e=0df19a944a
Registration: online; Deadline: one week before the event.
Location: online. After registration, you will receive the details of the ZOO meeting
For details and assistance info@avantyo.com, anca.bejenaru@avantyo.com