During the online round table organized by AVANTYO on August 7, 2020, at 13:00, the competent authorities will provide new information and solutions for the development of clinical trials in the conditions of the COVID-19 pandemic and the delays accumulated in the approval process.
Through a series of regular meetings with regulators, AVANTYO Institute of Clinical Research aims to facilitate new clarifications that will lead to improved development of clinical trials in our country.
"Regular meeting with regulators on the development of clinical trials in Romania" in August 2020 is the second online event organized by AVANTYO which brings together around the same table representatives of regulators, pharmaceutical companies and organizations conducting clinical trials in order to facilitate collaboration and find new ways to improve.
The host of the event will be Dr. Cristina Florescu Moraid - Director of AVANTYO Institute of Clinical Research.
On behalf of the National Agency for Medicines and Medical Devices of Romania (ANMDMR) will participate as special guests, Dr. Bujor Eugen Almașan - President, Dr. Mirela Vita - Head of Clinical Studies Department and Dr. Adina Pirvu - Inspector General Directorate of Inspection Pharmaceutics.
Prof. Dr. Constantin Mircioiu will represent the National Commission for Bioethics of Medicines and Medical Devices (CNCMDM)
Online registration is open until Thursday, August 6, 2020, at noon.
The event is free and will take place on ZOOM, in Romanian, for one hour.
Registration for event participants is done online at https://www.avantyo.com/roundtables/regular-meeting-with-authorities-aug2020. www.avantyo.com