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Bethesda North Marriott Hotel and Conference Center

Feb 03, 2025 7:45 AM - Feb 05, 2025 12:45 PM

5701 Marinelli Road, North Bethesda, MD 20852

Regulatory Submissions, Information, and Document Management Forum

Don't miss the latest trends, innovations, and best practices in regulatory submissions, information, and document management (RSIDM)!

Session 10: International Regulatory Authority Updates

Session Chair(s)

Lindsay  Fitzgerald

Lindsay Fitzgerald

Delivery Manager, Astrix, United States

Tamei  Elliott, MS

Tamei Elliott, MS

Director, Global Scientific Content, DIA, United States

Receive the latest updates from international regulators about recent and future developments. This session provides attendees the opportunity to ask regulators questions directly. Please note: due to the high volume of questions, not all will be answered live at the forum.

Kellen Cristina de Freitas Gissoni, ANVISA

Swissmedic Regulatory Update – DIA RSIDM Forum 2025 - Philipp Weyermann, Swissmedic

Karin Hay, Health Canada

International Regulatory Authority Update - Hilmar Hamann, European Medicines Agency

Learning Objective : At the conclusion of this session, participants should be able to:
  • Gain insights on recent updates and future developments from various global regulators

Speaker(s)

Kellen  Christina de Freitas Gissoni, RPh

Kellen Christina de Freitas Gissoni, RPh

Health Regulation Specialist, ANVISA, Brazil

Speaker

Philipp  Weyermann, DRSc, MSc

Philipp Weyermann, DRSc, MSc

Head of Unit Regulatory Assessment 2, Swissmedic, Switzerland

Swissmedic Regulatory Update – DIA RSIDM Forum 2025

Karin  Hay

Karin Hay

Senior Policy Analyst, Health Canada, Canada

Health Canada Update

Hilmar  Hamann, PhD

Hilmar Hamann, PhD

Chief Information Officer, European Medicines Agency, Netherlands

International Regulatory Authority Update – EMA

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