As you plan for RAPS Convergence 2025, expect focused time with more than 2,000 professionals who live the day-to-day of compliance and product development.
You’ll get expert-led sessions, direct dialogue with health authorities, and structured networking you can use immediately. The agenda blends emerging trends with practical how-to guidance—useful whether you’re planning a 510(k), IVDR strategy, or global post-market program.
Why 2,000+ Global Regulatory Professionals Choose RAPS Convergence
Each year, professionals from 50+ countries choose Convergence for rigorous content and peer exchange that translates into better submissions and cleaner audits.
You’ll expand your toolkit, compare approaches across markets, and benchmark against evolving standards.
With sessions tailored to every career stage and specialty, the event’s global scope exposes you to diverse strategies and proven practices that stand up to reviewer questions.
Educational Excellence and Expert-Led Sessions
Access sessions designed to sharpen strategy and execution—from evidence planning and labeling to clinical evaluation and lifecycle management.
Formats are led by regulators and industry experts, emphasizing what’s current, what’s changing, and what reviewers expect.
Interactive segments prioritize takeaways you can apply to active projects with confidence.
150+ Sessions Across Critical Regulatory Domains and Continuing Education
With over 150 sessions available, this conference delivers targeted learning across high-impact domains so you can meet compliance requirements and keep products moving.
You’ll build depth across four tracks—Medical Devices & IVDs, Pharmaceuticals & Biologics, Broad Interest, and Skill Building—organized for practical application.
Earn 15+ CEUs while strengthening core competencies.
- Deepen regulatory strategy skills with expert-led panels.
- Secure essential continuing education credits.
- Advance your career with targeted, skill-focused workshops.
Interactive Learning Formats and Global Health Authority Insights
Beyond the core tracks, you’ll engage through formats built for real-world problem-solving.
Health Authority Forums with FDA, EMA, and other regulators provide first-hand policy updates and expectations. “Conversations that Matter” enables live Q&A on thorny issues.
“Meet the Authors” connects you with RAPS publication experts, and Solutions Circles drive peer-to-peer troubleshooting so you leave with concrete, compliance-ready actions.
Networking and Career Advancement Opportunities
Convergence pairs strong content with structured networking to accelerate your next step.
You’ll find targeted career resources and mentorship that reflect the realities of regulatory work—shifting guidance, lean teams, and tight timelines. This is an excellent opportunity to build relationships that open doors and sharpen your judgment.
To maximize your experience:
- Connect with industry leaders during scheduled networking events.
- Participate in mentorship sessions focused on career development.
- Access workshops that address the latest trends and skills for career progression.
These moves compound—use them to strengthen your network and stay market-ready.
Pittsburgh Networking Events and Industry Innovation Trends
While the program centers on regulatory excellence, Pittsburgh’s venues add memorable settings for deeper discussions.
You’ll connect with peers against a backdrop of the city’s innovation culture while sessions tackle digital transformation, global harmonization, and regulation of emerging technologies.
Expect practical dialogue that links policy to execution. The result: clearer decisions, stronger documentation, and relationships that help you navigate what’s next.
This event blends local energy with forward-looking content to support confident leadership in regulatory affairs and MedTech innovation.
Frequently Asked Questions:
What Are the Conference’s Exact Dates, Location, and Registration Deadline?
The conference will be held from October 7 to 9, 2025, at the David L. Lawrence Convention Center in Pittsburgh, Pennsylvania. Preconference workshops will run from October 6 to 7.
Advanced registration pricing is available through August 26, 2025, allowing attendees to secure reduced rates before standard pricing begins.
What Are the Registration Costs and What’s Included in Each Package?
Registration ranges from core conference access to all-inclusive packages featuring workshops, networking events, and CEU opportunities.
Advanced rates offer tangible savings, giving professionals the flexibility to balance budget with value while ensuring full access to sessions and resources tailored to career stage and focus areas.
How Many Continuing Education Credits Can I Earn?
Attendees can earn over 15 continuing education units (CEUs), supporting RAC maintenance and other certifications.
Sessions are structured to provide relevant credit based on your practice area, making it a practical way to advance professional knowledge while aligning with evolving regulations and compliance standards.
How Will the Conference Address Current Regulatory Technology and AI Trends?
It includes sessions on AI applications in regulatory workflows, cybersecurity for connected medical devices, and practical RegTech tools for digital submissions.
Discussions also cover breakthrough device pathways, offering real-world insights into how emerging technologies reshape regulation frameworks and compliance strategies worldwide.
What Makes Pittsburgh an Ideal Location for This Conference?
Pittsburgh offers convenient access for over 2,000 international attendees and a rich mix of cultural and professional venues. Sites like Acrisure Stadium and the Heinz History Center complement conference programming, fostering meaningful networking while balancing professional and cultural engagement.
Conclusion
Attending RAPS Convergence 2025 positions you at the forefront of regulatory excellence and MedTech innovation. Gain actionable insights from global authorities, participate in compliance-focused discussions, and expand your professional network through structured events.
With over 2,000 peers and 150+ sessions, you’ll stay ahead of emerging trends, regulation changes, and industry best practices, strengthening your expertise and advancing your career in a dynamic, collaborative environment.
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DISCLAIMER: While we do our best to keep the information on our website accurate and up-to-date, it’s important to note that this content may change and isn’t intended to be medical or legal advice. All information is provided for general use and might not apply perfectly to every situation. We encourage you to contact us to discuss how this topic applies to your specific situation and get more personalized guidance.