RP360 Academy

Master medical device safety & regulatory affairs.

The Academy is an expert-led learning platform for medical device professionals, spanning regulatory affairs, quality systems, risk & safety, and post-market intelligence.

Free foundational courses — no payment required to start.

Tracks

Regulatory Affairs · Quality Systems · Risk & Safety · Post Market Intelligence

Exam prep

Exam-aligned simulator with a rationale on every answer

Certifications

Shareable digital certifications

Pricing

Free courses to start · contact us for pricing

Structured tracks

  • Regulatory Affairs — FDA · MDR · 510(k) · Global Submissions
  • Quality Systems — CAPA · Complaint Handling · ISO 13485 · Internal Audits
  • Risk & Safety — Risk Management · FMEA · Human Factors · Design Controls
  • Post Market Intelligence — Trending & Analytics · PMS · MDR Reporting