Regulatory Affairs - Clinical Trials Information System in Europe (EMA-Clinical Research). Peivand Pirouzi, Ph.D.

In this video, Professor Peivand Pirouzi provides an in-depth look at the Clinical Trials Information System (CTIS), a crucial initiative by the European Medicines Agency (EMA) that aims to streamline and enhance the management of clinical trials across Europe. With the implementation of this system, the regulatory environment for clinical research in Europe is evolving, providing new opportunities and challenges for researchers and sponsors alike.

Key topics covered include:

An overview of the Clinical Trials Information System (CTIS) and its role in clinical research
How the EMA is improving the submission, assessment, and supervision of clinical trials through CTIS
Key features and functionalities of the CTIS platform for clinical trial sponsors and researchers
Navigating regulatory requirements and compliance in clinical research within Europe
The impact of CTIS on transparency, patient safety, and data management

This video is a valuable resource for researchers, clinical trial managers, and regulatory affairs professionals working in Europe or with European clinical trials. Professor Pirouzi provides insights into how to leverage CTIS for effective and efficient clinical trial management.