The EFPIA has revealed the appointment of Nathalie Moll as its new director general.
The European Federation of Pharmaceutical Industries and Associations (EFPIA) has revealed the appointment of Nathalie Moll as its new director general. Currently secretary general of the European Association for Bioindustries (EuropaBio), she will join EFPIA in April 2017.
Commenting on the appointment, Joe Jimenez, President of EFPIA, said “Nathalie has an excellent track record of leadership and engagement across the life science sector. We are confident she is the right person to lead EFPIA, working with stakeholders to address the challenges faced by healthcare systems in Europe.”
Moll became secretary general of EuropaBio. Moll, currently EuropaBio’s director for agricultural biotechnology in April 2010, replacing Willy De Greef.
“I am delighted to be joining EFPIA at a time when pharmaceutical innovation is having such a dramatic effect on the lives of patients across Europe,” she said. “I look forward to working with EFPIA Members, staff and the wider research, healthcare and policy community to foster an environment that supports continued innovation and drives better outcomes for patients.”
Eric Cornut will continue to lead EFPIA as interim director general until Moll joins the organisation in April.
Philip Ward is the European Editor for Applied Clinical Trials
Empowering Sites and Patients: The Impact of Personalized Support in Clinical Trials
November 26th 2024To meet the growing demands of clinical research, sponsors must prioritize comprehensive support models, such as clinical site ambassadors and patient journey coordinators, who can address operational challenges and improve site relationships, patient satisfaction, and overall trial efficiency.
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.
FDA Finalizes Decentralized Clinical Trial Guidance
November 25th 2024The FDA's guidance is part of a broader effort to modernize clinical trials, improve efficiency, reduce participant burden, and expand access, particularly for underrepresented populations and those in geographically or economically constrained areas.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.