Upcoming Events

Designed for senior regulatory leaders, this program sharpens high-level communication, strategic decision-making, and risk management skills. It equips participants with proven techniques to align stakeholders, foster inclusion, and navigate complex, high-stakes environments with clarity and confidence.

Stay ahead of rapidly changing global cybersecurity requirements for medical devices. This two-day interactive workshop will provide regulatory, quality, and technical professionals with the tools and knowledge needed to address cybersecurity risks, strengthen regulatory submissions, and meet expectations from health authorities worldwide that you can apply immediately.

In our last session on XaaS and AI, we presented an approach for implementing cloud and AI technologies in regulated environments. The natural next question is: where does an organization begin? For regulatory affairs professionals, the answer comes back to one thing: how well your regulatory information is structured and managed. In this session, we will explore a system built with this exact objective in mind: the Regulatory Information Management (RIM) system.

Participating in RAPS France LNG in person social event is the perfect opportunity to expand your network and share your insights on topics most relevant to health products. Interested CE marking process? You will also have the opportunity to speak to GMED team who kindly sponsored this event.

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

With dedicated programme streams for human medicines (pharmaceuticals), medical devices, IVDs and veterinary medicines, the Symposium is the must-attend event in the regulatory affairs calendar.

Vorträge und eine Paneldiskussion über Regulatory Affairs im digitalen Wandel. Seien Sie bei dieser spannenden Diskussion dabei!

Join RAPS Twin Cities for an interactive keynote on what separates regulatory leaders who truly move the enterprise, with Jackie Peterson, PCC, CEO of Lift Bridge Leadership. Leave with one committed action.

Join RAPS Philadelphia for an in-person panel on pediatric rare disease drug development. Explore evolving regulatory strategies, innovative evidence generation, patient engagement, and practical approaches to advancing therapies for children.

Health Canada Medical Device Single Audit Program (MDSAP) Advancements

Join us for a networking and recruitment series across multiple in-person events. Meet regulatory professionals, connect with chapter leaders, and learn about ambassador and leadership roles.

This 4-hour virtual workshop compares FDA, EU, MDSAP, NMPA, MFDS, and PMDA expectations, inspection trends, documentation requirements, and responses to findings, using case studies to strengthen global inspection readiness and compliance.

Join RAPS Philadelphia for a cross-functional look at leveraging business and legal topics to supercharge your regulatory intelligence, drive product development insight, and communicate value effectively across your key stakeholders. In a program sure to be insightful for regulatory and legal professionals alike, an expert group of panelists will discuss strategies and practical takeaways to bring back to your business.

Build practical AI literacy skills for regulatory affairs through hands-on exercises and group discussions. Learn where AI can add value, understand its risks, and apply it responsibly across the regulatory lifecycle.

Updates to Annex VII of the EU MDR 2017/745 reshape notified body requirements and their impact on manufacturers. This webcast reviews the changes, their rationale, and implications for organizational structures, competencies, certification activities, and timelines, providing practical insights to support MDR compliance and certification readiness.

Explore responsible AI governance in GxP-regulated environments, covering risk, validation, data integrity, oversight, and how the EU AI Act and ISO/IEC 42001 align with existing quality frameworks.

Join the TEAM-PRRC Annual Summit 2026 in Prague, the key European event dedicated to PRRCs (Persons Responsible for Regulatory Compliance) and regulatory affairs professionals in the medical device sector.

Join SGS & RAPS for a dynamic full-day event focused on advancing medical technology and providing greater protection for patients, featuring multiple FDA speakers and medical device industry experts.

Learn how AI-enabled CER workflows can help regulatory teams improve efficiency, traceability, and MDR compliance while strengthening Notified Body readiness and preserving expert oversight.

Join us at UCI for an in-person evening event for students. Attendees will learn how graduate training connects to regulatory affairs careers in healthcare, hear from senior regulatory leaders, and gain practical advice on positioning their skills for hiring managers.

Building on the momentum of the inaugural “From Classroom to Career” panel held in May 2026, the RAPS NC Local Networking Group returns to continue the conversation on clinical research and regulatory affairs workforce development in North Carolina and beyond. This second installment brings together industry leaders, academic faculty, and emerging professionals to revisit the state of regulatory and clinical research education: what progress has been made since the spring discussion, where gaps still persist, and what new curricular innovations are shaping the pipeline of talent entering the field. Panelists will examine how academic programs are adapting to industry demand, the role of mentorship and experiential learning in preparing students for regulatory careers, and strategies for strengthening the connection between classroom instruction and real-world practice. This event is designed for clinical research professionals, regulatory affairs practitioners, academic faculty, students, and anyone invested in shaping the educational infrastructure that supports these fields.

Overview of chemistry, manufacturing and control (CMC) regulatory requirements and best practices associated with biologics. Emphasis on requirements in US, Europe, and other regions.

Gain confidence in implementing the EU MDR! Receive useful advice on updating your quality system, overseeing economic operators, addressing labeling, and handling technical documentation.