Conferences, trade shows, training and webinars on MDR, IVDR, ISO 13485, FDA and more. The reference calendar for medical device professionals.
The North Carolina RAPS local networking group is pleased to present a panel discussion featuring industry leaders and academic professors to examine the current landscape of education in clinical research and regulatory affairs in North Carolina and beyond.
This session offers practical lessons learned from interactions with the FDA regarding software, algorithms, AI/ML, and cybersecurity in safety-critical medical devices.
The North Carolina local RAPS networking group presents an in-person session of the FDA's ASCA program focused on the appropriate use of standards, compliance assessment, and practical strategies for pre-market submissions.
A deep dive into European Medical Device Regulation (MDR)
Join a series of RAPS networking and recruitment meetings across several in-person events. Meet regulatory professionals, connect with chapter leaders, and learn more about ambassador and leadership roles. Build your network and support the local regulatory community.
Preparing a successful 510(k) requires more than just completing a template — it necessitates a clear regulatory strategy, thoughtful planning, cross-functional coordination, and a deep understanding of FDA expectations. Join regulatory consultant Nancy Sauer for a practical discussion on best practices for 510(k) submissions, common pitfalls, and lessons learned from working with the FDA.
Join the NJ and Philadelphia chapters as we host FDA and Intertek speakers discussing FDA’s Accreditation Scheme for Conformity Assessment (ASCA) and how it streamlines premarket review by elevating the quality and consistency of testing laboratories, enabling reviewers to assess complex areas like biocompatibility and EMC in minutes rather than hours. This session explains how ASCA reduces deficiencies, protects test data integrity, and demonstrates through real case studies how submissions once stalled for months can move forward in weeks.
This RAPS online training is designed to support students and early-career professionals seeking to better understand career opportunities in regulatory affairs and adjacent fields.
A deep dive into European Medical Device Regulation (MDR)
This RAPS training is designed to support students and early professionals seeking to better understand career opportunities in regulatory affairs and adjacent fields.
This webinar explores how quality management systems evolve throughout the lifecycle of the organization - from lean startup environments to complex global enterprises. Participants will gain practical insights on balancing speed and compliance, designing scalable processes, while navigating resources as well as regulatory and cultural challenges at different stages of growth.
Join RAPS Pittsburgh LNG and Nucleate Pittsburgh for a free hour of networking at Local Remedy Brewing. Connect with biotechnology innovators, students, entrepreneurs, and regulatory affairs experts.
Practical session on the biological evaluation of medical devices: expectations of ISO 10993, US FDA, and European MDR, and chemical characterization.
This workshop is designed to assist regulatory and product development teams in successfully bringing AI/ML medical devices to market.
The Gulf Pharma Regulatory Affairs Summit is the annual event in the region dedicated exclusively to pharmaceutical regulatory affairs in the Gulf. The summit brings together regulatory authorities, registration experts, and leaders in the pharmaceutical industry to discuss the latest developments in drug registration, market authorization, regulatory news, and compliance frameworks in the GCC.
Join SGS and the Boston Chapter of RAPS for a high-impact symposium dedicated to critical risks and regulatory challenges affecting pharmaceutical and medical supply chains in 2026 and beyond.
Find out if the new RAPS FRA accreditation without prior experience is suitable for your professional profile.
International medical technology trade fair in Southeast Asia, Singapore.
Join this free webcast to find out whether RAC credential is right for you and how to get started. Discover how earning this globally recognized certification can boost your earning potential and your regulatory career.
In this webcast, you will learn how to secure your role as an EU compliance professional. Discover the essential steps to earning the RAPS Regulatory Compliance Certification.
Discover how to enhance your pre-market success with the FDA's ASC and UL solutions.
Join expert speakers and experienced professionals for a full-day, hands-on workshop where you will explore practical applications of Artificial Intelligence, from analytics supporting regulatory intelligence to building custom GPTs and drafting effective invitations.
Join the Medicen event dedicated to financing Medtechs in 2026. Discover the impact of CE marking on valuation, investor expectations, and strategies to successfully raise funds.
Join the RAPS Twin Cities Chapter for our annual symposium, a full-day event that brings together regulatory professionals, industry leaders, and subject matter experts for an in-depth exploration of the most critical medical regulatory topics of 2026.
This interactive workshop provides practical Notified Body insights on how manufacturers can build, maintain, and evaluate risk management documentation compliant with EU MDR/UKCA and the outputs of IFU/labeling related to ISO 14971 and FDA QMSR.
Exclusive RAPS-SF event for VPs and above. This facilitated roundtable provides an intimate and interactive environment for senior professionals to unpack the monumental changes at the FDA, share strategic plans, and candidly discuss what the "new normal" at the FDA means for our industry.
Practical session on the biological evaluation of medical devices: expectations of ISO 10993, US FDA, and EU MDR, and chemical characterization.
Join RAPS Ontario for our Summer Meeting, featuring an exciting Speed Networking session and inspiring career conversations. Connect with regulatory professionals, students, and industry leaders. Hear diverse career stories, expand your network, and enjoy light snacks and refreshing beverages in a relaxing and welcoming environment.
Educational and networking event for students in Southern California to explore our professional support in the regulatory and quality community.
The IPSF EuRS is the key regional event of the IPSF EuRO organized annually for pharmacy students and recent graduates, particularly focused on the European region.
The 10th edition of the summit brings together manufacturers, authorized representatives, notified bodies, regulators, legal experts, policy stakeholders, and industry leaders to discuss the practical realities of implementing the MDR and IVDR.
Two days of training on the regulatory news of medical devices: MDR, IVDR, AI and health. Exhibitor village (34 stands) bringing together notified bodies, laboratories, consulting firms, and training organizations.
This workshop addresses the potential gaps in the ISO 13485:2016 standard to prevent cybersecurity threats and ensure data integrity.
MedTech, diagnostics, and e-health business convention. 10th anniversary in Marseille.
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