RP360 Academy · Medical Device Safety Intelligence

Become the professional
who catches risk first

Master medical device safety, regulatory and risk intelligence — from your first FDA course, to leading your organization’s shift from reactive compliance to prediction. Learn. Lead. Predict.

Explore the Academy Executive Masterclass

Leading a team or evaluating tooling? RP360 for organizations →

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Start where you are

One mission. A path for everyone.

Most people start in the Academy. Leaders join the Masterclass. Organizations adopt the Platform.

Learn · Start here

RP360 Academy

Expert-led education across regulatory, quality, risk and post-market intelligence — free foundational courses, certifications, RAC exam prep, and deep learning tracks.

  • 4 structured tracks · expert-led courses
  • Free foundational courses & certifications
  • RAC exam simulator and study guides
Explore the Academy Plans from $49/mo
Lead · Executive Masterclass

Executive Masterclass

A live cohort on leading the shift from reactive compliance to predictive safety intelligence.

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Predict · For Organizations

RP360 Platform

Enterprise risk intelligence — detect emerging risk earlier across your device portfolio.

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Find your journey

Regulatory Professional

Advance your knowledge and build your career.

Go to Academy

Quality & Safety Leader

Stay ahead of risk and strengthen your teams.

Join the Masterclass

Enterprise

Detect risks earlier and make better decisions.

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Built for professionals across the medical device industry
CardiovascularOrthopedicsDiagnostic ImagingSurgical RoboticsIn-Vitro DiagnosticsCombination ProductsClass III ImplantsDigital HealthCardiovascularOrthopedicsDiagnostic ImagingSurgical RoboticsIn-Vitro DiagnosticsCombination ProductsClass III ImplantsDigital Health

Frequently asked questions

What is RP360?
RP360 is a medical device safety ecosystem with three connected offerings: the Academy (expert-led education in regulatory, quality, risk and post-market intelligence), the Executive Masterclass (a live cohort for leaders), and the Platform (enterprise risk-intelligence software). The through-line is helping teams move from reactive compliance to predicting risk earlier.
Who is RP360 for?
Professionals and organizations across the medical device industry — from regulatory and quality specialists advancing their careers, to Quality & Safety leaders building stronger teams, to enterprises detecting portfolio-wide risk earlier. It spans device areas including cardiovascular, orthopedics, diagnostic imaging, surgical robotics, in-vitro diagnostics, combination products, Class III implants and digital health.
Where should I start — Academy, Masterclass, or Platform?
Most people start in the Academy with free foundational courses. Directors and VPs leading a shift toward predictive safety join the Executive Masterclass. Organizations evaluating tooling adopt the Platform. You can start free in the Academy today and explore the others when you're ready.
Do I have to pay to get started?
No. You can create a free account with no credit card and begin with foundational courses (including FDA Fundamentals), course previews, and an exam preview. Paid plans and cohorts unlock the full library, live classes, and certifications.
Is RP360 only about FDA/US regulations?
No. While FDA topics such as 510(k), QSR, Warning Letters and MAUDE feature heavily, the Academy's tracks also cover global submissions, EU MDR, ISO 13485, risk management and post-market surveillance relevant to manufacturers operating internationally.
What does moving from reactive compliance to prediction mean?
Traditionally, safety and quality work responds to problems after they surface. RP360 teaches skills and provides tooling that help teams spot weak signals early — across complaints, adverse-event data and literature — so emerging risk is caught and acted on before it becomes a recall.