EMR and eISF in clinical trials - how, why, when and where?

Ukrainian Association of Clinical Research (UACR) in collaboration with Association of GCP Poland (GCPpl) would like to invite you to attend the webinar: 

"EMR and eISF in clinical trials - how, why, when and where?"

The main goal of the webinar is to look at electronic medical records (EMR) and electronic Investigator Site File (eISF) in a pragmatic way and to share the experience on EMR and eISF between participants that is why active participation will be appreciated.

WEBINAR details:

• Date: 11May2021
• Time: 12:45 - 15:00 (CEST)
• Target participants: all clinical trial professionals
• Webinar will be conducted in English
• Participation in the event is free of charge

AGENDA:

12:45 - 13:00 - Registration

13:00 - 14:00 - Part I: Electronic Medical Records - how and where to start, current experience, main risks, regulatory requirements / 20 min. intro and 40 min. of discussion / Anna Titkova, MD, PhD, Prof., MBA (CEO and Director of Operations, Pratia Ukraine), Joanna Job, MSc, ACRP-CP, MRQA (Global Operational Compliance Manager, Pratia)

14:00 - 15:00 - Part II: Electronic Investigator Site File - how to start, what are the possibilities, what is the impact / 20 min. intro and 40 min. of discussion / Ivan Vyshnyvetskyy, MD, PhD (President, Ukrainian Association for Clinical Research; Research Director, EBM&GCP Research Institute LLC)