Upcoming Events

A seminar tailored for regulatory affairs professionals and promotional review teams in life sciences. We’ll explore the evolving FDA landscape on advertising and promotional enforcement, along with recent guidance.

This panel brings together seasoned regulatory leaders, innovators, and industry strategists to explore how early‑stage companies can build the right foundations for long‑term success.

Join the launch of RAPS Poland LNG. Explore the RAPS Poland LNG, meet our leaders, discover RAPS benefits with Kim Young, and connect with regulatory professionals from pharma, medical devices, and cosmetics.

This Summit is a strategic meeting place in the GCC region for local and international pharmaceutical and medical industry professionals to meet and discuss on topics related to all aspects of regulatory affairs, legal and compliance.

This intensive 16-hour course, delivered across 4 half days, will give you an excellent grounding in the EU requirements for clinical evaluation.

Explore the evolving regulatory landscape for CGT combination products focusing on device development and potency assay requirements.

MedCon unites the healthcare products community for unparalleled regulatory and industry collaboration. The event facilitates a neutral setting for information sharing to drive a common understanding of key regulatory and quality concepts.

This session will demonstrate the value of standards, explain how to cite them to maximize efficiencies, describe the process for an ASCA test and how the industry uses ASCA.

This leading event unites the Medtech industry's regulatory and quality experts for educational sessions and networking opportunities. Participants will have the chance to interact with Health Canada and other key players in a collaborative setting.

Explore regulatory strategies for medical device start-ups, including FDA pathways, early planning, and building effective quality systems..

Please join us for this informal event meant to connect our chapter members to each other and build our professional networks.

AI-enabled medical devices must meet overlapping FDA, EU MDR, and EU AI Act requirements. Learn to operationalize compliance with shared data and AI to reduce manual work and accelerate audit-ready submissions.

This session explores how current regulatory leaders can intentionally shift from being technical experts to becoming talent multipliers within their organizations.

This webcast will demystify the Human Factors Use-Related Risk Analysis (URRA), explain why it is often misused, and share a proven approach to build and apply URRA distinct from other risk management tools.

A fireside chat on AI in regulatory affairs, covering document drafting, regulatory intelligence, safety monitoring, and compliance review, while also addressing privacy, security, and integrity risks.

This hands‑on workshop demystifies IVDR and CTR requirements, empowering regulatory professionals to confidently navigate today’s evolving precision‑medicine landscape to better clarify biomarker-driven drug development.

Join us for a panel discussion about the unique considerations that can impact regulatory activities throughout the lifecycle of a combination product with a device constituent part for delivery of a drug or biologics.

Discuss regulatory intelligence platforms’ critical role in the practice of regulatory science, allowing regulatory professionals to work more efficiently without compromising scientific rigor or judgment.

Explore the unseen risks at the intersection of Medical Information and Pharmacovigilance.

The upcoming 4th Edition of the IEC 60601 1 standard represents a significant evolution in the regulatory expectations for medical electrical equipment and medical electrical systems. This presentation will highlight the major conceptual and structural changes being introduced, with a focus on how these updates may impact design, documentation, and compliance activities for manufacturers and system integrators.

Utah RAPS Chapter St. George Event at Utah Tech

Learn from faculty at one of the world’s most prestigious business schools in an environment dedicated to preparing regulatory leaders.

Workshop virtual explora aplicações, oportunidades e desafios da inteligência artificial em Assuntos Regulatórios e tomada de decisão

RAPS Euro Convergence is the most comprehensive regulatory affairs conference in Europe, focusing on the latest topics and developments in healthcare products in Europe and beyond!