A Practical Guide to EU Market Approval for Medical Software
RAPS Nordic session with Health Tech Pathways and Scarlet: a practical introduction to navigating the EU MDR for medical software.
Evolving QMS Maturity: Regulatory Strategies from Emerging Companies to Global Enterprises
RAPS Seattle virtual event on how quality management systems evolve as a medical device company grows. 1 CE credit. Date:
Standards in Action: FDA’s ASCA Program, From Test Lab to Premarket Review
RAPS New Jersey and Philadelphia chapters host FDA and Intertek on how ASCA test reports are used in premarket review.
Mastering the 510(k): Practical Strategies for Success with eSTAR
RAPS Colorado Chapter virtual event on preparing a 510(k) submission in eSTAR, beyond simply completing the template. 1 CE credit.
Inside FDA ASCA: Practical Insights
RAPS North Carolina session on the appropriate use of standards under the FDA Accreditation Scheme for Conformity Assessment. 2 CE
MDR 2.0: Understanding the What, Why, How, When, Where, and Who
RAPS Austria virtual event: a deep dive into the proposed revision of the European Medical Device Regulation. 1 CE credit.
When AI Hallucinates: From Architectural Root Cause to Auditable Solutions for Regulated Industries
RAPS Boston Chapter virtual event on why AI systems hallucinate and what an auditable solution looks like in a regulated
MedTech Summit 2027
Informa’s regulatory conference for the medical device and IVD sectors, covering EU MDR and IVDR implementation. Date: 2027-06-07 to 2027-06-10
CAPRA 2026 Annual Symposium
The Canadian Association of Professionals in Regulatory Affairs annual symposium. Date: 2026-12-01 to 2026-12-02 Location: Toronto, Canada Event details and
Combination Products Summit 2026
RAPS summit on drug-device combination products, covering regulatory strategy and innovation. 12 CE credits. Date: 2026-11-17 to 2026-11-18 Location: Baltimore,