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Your membership opens the door to free learning resources on demand. Check out the Member Knowledge Center for free webcasts, publications and online courses.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
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The most valued regulatory professionals are more than technically competent. They have multiple regulatory voices depending on the situation—team member, leader and facilitator—especially across a wide array of health authority, compliance, cultural, ego, cross-functional and developmental issues.
Learn the professional development skills you need for success, including how to advance these critical skills and how to improve the power of your regulatory voices strategically. This will be discussed in the context of the various roles regulatory professionals play in different scenarios, teams and companies.
Intermediate: Content is designed based upon the assumption that individuals have basic knowledge of the topic(s) and/or demonstrated competence related to the topic(s). Higher-level concepts are introduced during lectures; exercises requiring synthesis and/or application of concepts are incorporated into the activity.
Upon the webcast's conclusion, you will be able to:
Who Should Attend?
Michael J. Vivion, PhD, principal, ECG Inc.
Michael J. Vivion, PhD, has a long record of success in dealing with regulatory agencies in the US, Canada, Europe, Japan and China on behalf of both new and existing pharmaceuticals, devices, biologics and vaccine products. Previously, Vivion was global head of strategic communications for F. Hoffmann-La Roche in Basel. He worked with numerous teams to help develop communication strategies and tactics in therapeutic areas ranging from HIV to oncology and allergies to obesity. Vivion continues his appointment as a visiting lecturer on regulatory communication for the European Centre of Pharmaceutical Medicine at the University of Basel. He is also a frequent speaker at major business and university conferences.
Beth Weinberg, RPh, advisor, global regulatory affairs - North America, Eli Lilly and Company
Beth Weinberg has held various roles at Eli Lilly and Company during her 20 year career including clinical, scientific communications and in advertising/promotion and development regulatory affairs. She has worked across many therapeutic areas and currently focuses on diabetes drugs in development. Weinberg has supported both marketed products and drugs in development and has successfully managed key New Drug Application (NDA) supplements, including labeling, Chemistry, Manufacturing and Controls (CMC) and 505(b)(2) applications. Previously, Weinberg worked as an executive sales representative for Abbott Laboratories.
Jacques C. Mascaro, senior vice president, global regulatory affairs and R&D quality assurance, Merck Serono
Questions? Call the RAPS Solutions Center at +1 301 770 2920, ext. 200, or email email@example.com.