Eleonora De Pascali
About Eleonora De Pascali
Eleonora De Pascali is a Manager of Regulatory Affairs at Bristol-Myers Squibb in New Jersey, United States, with over a decade of experience in the pharmaceutical industry.
Current Role at Bristol-Myers Squibb
Eleonora De Pascali currently holds the position of Manager Regulatory Affairs at Bristol-Myers Squibb in New Jersey, United States. In this role, she is responsible for overseeing regulatory strategies and ensuring compliance with regulatory requirements within the pharmaceutical industry. Her contributions are significant in maintaining the regulatory standards of the organization, which is crucial for the development and distribution of pharmaceuticals.
Experience in Regulatory Affairs
Eleonora De Pascali has over a decade of experience in regulatory affairs, specifically within the pharmaceutical industry. She has been dedicated to this field since at least 2013, bringing extensive knowledge and expertise to her current role. Her specialization in regulatory compliance has been instrumental in navigating complex regulatory environments and ensuring the successful approval and market entry of pharmaceutical products.
Previous Position at Italfarmaco S.p.A.
Before joining Bristol-Myers Squibb, Eleonora De Pascali served as a Regulatory Affairs Specialist at Italfarmaco S.p.A. In this capacity, she was involved in managing regulatory submissions, maintaining compliance with regulatory guidelines, and supporting the company's efforts to bring new pharmaceutical products to market. Her role at Italfarmaco provided her with critical experience and a strong foundation in regulatory affairs.
Specialization in Pharmaceutical Regulatory Affairs
Eleonora De Pascali specializes in regulatory affairs within the pharmaceutical industry. Her expertise includes developing regulatory strategies, preparing and submitting necessary documentation to regulatory authorities, and ensuring that all processes meet regulatory standards. This specialization has equipped her with the skills needed to navigate regulatory challenges and contribute to the successful introduction of new pharmaceutical products.