Thursday, November 7th, 2019 - Bruxelles
Official language: English
The way how Clinical Trials are run is entering extraordinary times.
Evolutions in technology, regulations and processes bring along unprecedented challenges and opportunities for all parties involved. For the patients and their caregiver, the sites, the health care professional, the regulator, the sponsor, the vendors and CROs.
During the Benelux ePharma Day we bring all stakeholders together and will have discussions on topics ranging from common pain points to sharing best practices. We will discuss on how to ensure Benelux remains an attractive environment for Clinical Trials.
It is a great opportunity to meet top experts and decision makers from Patient Associations, Regulatory Agencies, Academic Institutions, Clinical sites, CROs, and Pharma Industry to exchange ideas, to interact and network.
Following questions will be addressed:
Prof. Laetitia Huiart - Director of the Department of Population Health at Luxembourg Institute of Health
Isabelle Van Der Haegen - Country Head Belgium/Western European Supporting Markets Country Clinical Operations at Roche
Griet Goddemaer - Executive Director Clinical Operations, EMEA North Cluster at Covance
Representatives of Pharmaceutical and Biotechnology companies, Clinical Research Organizations, Academic centers, Hospital Centers, and Clinical Technology companies. Especially Clinical Research Professionals, belonging to the following departments:
• Clinical Research and Development
• Quality Assurance
• Clinical Operations
• Statistics and Data Management
• Information Technology
• Market Access
A portion of the proceeds from this event are donated to the “Vase of Flowers” project