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Regulatory Saturdays: EU-MDR Simplified!

Master EU-MDR Essentials in 6 weekends

Boost your regulatory skills with our compact weekend program. Weekly hands-on sessions deliver practical experience and solid EU-MDR knowledge to advance your career or ace credential exams.

SESSION DETAILS

📅 Start Date: January 10, 2026
📅 End Date: February 14, 2026

🎓 Mastery Session: February 15, 2026


🕒 Timing: Saturdays | 9:00 AM – 11:00 AM (ET)
💻 Platform: Online​

PRICE DETAILS

💰 Price: $99 CAD

🎓 Student Offer: Get the course for a flat $70 CAD

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👥 Bring a Friend: Enroll together & save 5% each

  Click “Let’s Chat” and request your discount code instantly.​​

Program Overview

An in-depth exploration of the weekly topic through guided instruction, practical examples, and regulatory insights.

A brief overview of the weekly topics is provided below. For a detailed breakdown, please refer to the Program Breakdown Brochure.

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  • Week 1 - EU-MDR Essentials: Structure, key players & Core concepts 

  • Week 2 - Classification & Conformity Assessment Foundations

  • Week 3 - Selecting the Conformity Assessment Route

  • Week 4 - Clinical Evaluation & EU Registration systems 

  • Week 5 - Clinical Investigations

  • Week 6 - Post-Market Surveillance

  • 12+ hours of live training
     

  • Live demos & real-world MDR activities
     

  • Hands-on EU-MDR assignments
     

  • 6 quizzes (20 questions each)
     

  • 2 practice tests (120 questions each)
     

  • Guest lectures
     

  • Certificate of Learning*
     

  • Missed a class? Recording provided

*Disclaimer:

RegStalk is not affiliated with RAPS or the RCC-MDR certification in any way. All study materials, quizzes, and practice exams are independently developed and are solely intended to support learning the EU Medical Device Regulation (EU-MDR).

These resources do not reflect the content, structure, or format of the official RCC-MDR exam and are not designed to replicate the exam. Their purpose is purely to help participants understand and apply the regulation.

Gautameee Cloudry Thyagaraj, Regulatory Affairs Consultant, Self-Employed

Regulatory document has difficult jargons to understand whereas Nivedha has made it simpler through her sessions.
So, now I'm able to easily interpret the regulatory language in the EU MDR guidelines and thus, making my exam preparation much faster. The power point presentations and the training materials are structured really well and helpful to revise on last week of the exam.
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