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Regulatory Saturdays: EU-MDR Simplified!

Master EU-MDR Essentials in 6 weeks

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—without overwhelm. Why gulp it when you can grasp it, week by week?

SESSION DETAILS

📅 Start Date: August 30, 2025
📅 End Date: October 4, 2025

🎓 Mastery Session: October 5, 2025


🕒 Timing: Saturdays | 9:30 AM – 11:30 AM (ET)
💻 Platform: Online

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PRICE DETAILS

💰 Price: $100 CAD

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🔥 DEAL: REGISTER TODAY FOR🔥
 

Only CAD 75 

EXTRA DISCOUNTS

​🎓 Student Special – Learn for just $60 CAD! - 

👥 Bring-a-Friend Bonus – Enroll together and both save 5% more 

💬Tap the chat icon now to request your exclusive coupon code.

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All Registrations close by August 29, 2025​

Note: 

  • ⏰ All sessions are conducted online. Check your local time using our Time Zone Converter.

  • 💱 Not in Canada? Use this Currency Converter to view prices in your approximate local currency.

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  • High Quality Lectures

  • 12+ hours live Training

  • Access to training materials

  • Live demos & real-world MDR scenarios

  • Hands-on EU-MDR Assignments

  • 6 Quizzes - 20 questions each

  • 2 Practice Tests - 120 questions each

  • Guest Lectures

  • Forum For Collaboration & Networking

  • Customized Support & Feedback

  • Certificate of Learning

  • Missed a class? Recordings provided

  • Structured to support exam prep for regulatory credentials like RCC-MDR *

*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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