Meet your Match: Regulatory Affairs

Friday, June 28, 13:45 - 14:45


About Francisco Hernandez | Pfizer

Francisco Hernandez is the Regulatory lead for Pfizer in the Netherlands. Responsible for the successful registration of the 1st and most successful mRNA Covid-19 vaccine in the Netherlands. Extensive expertise in regulatory affairs, and pharmaceutical policy. Before joining Pfizer, Francisco worked at the Dutch registration authority (CBG). Francisco has also knowledge and is extremely interested about the challenges with respect to access and their processes (e.g., market access, pricing, and reimbursement). He has a comprehensive knowledge of the drug development process from preclinical to post-marketing phases. Energetic advocate of diversity, equity, and inclusion. Sociable, multidisciplinary, creative, analytic, and versatile pharmacist and pharmaco-epidemiologist with heart for understandable and attractive information to educate patients and assist prescribers. Passionate leader and a people’s manager with focus on excellence, efficiency, nurturing, equity, and joy.




Pfizer

At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products, including innovative medicines and vaccines. To learn more, please visit us on www.Pfizer.nl and follow us on Twitter at @PfizerNL, LinkedIn and like us on Facebook at Facebook.com/pfizernederland.


Meet your Match: Regulatory Affairs

In this Meet your Match session, you will experience an in-depth look at Regulatory Affairs and explore the unique aspects of this dynamic career path. The session dives into the day-to-day responsibilities, work-life balance, salary expectations, flexibility, and career progression within the Regulatory Affairs field. You will gain insights into how these roles operate within the healthcare industry, providing a comprehensive understanding of what to expect.

During this session, the discussion will cover the core tasks and responsibilities of a Regulatory Affairs professional, highlighting the skills and expertise required for success. You will learn about the nuances of the job, from compliance and regulatory submissions to collaborating with cross-functional teams.

The informal session format offers ample opportunities for interaction and questions, allowing attendees to engage with experienced professionals and uncover what it truly means to work in Regulatory Affairs. For those considering a career in this field or seeking to expand their knowledge, this session is the perfect opportunity to explore career options and find a match.

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