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Regulatory Saturdays: EU-MDR Simplified!

Master EU-MDR Essentials in 6 weeks

 Ready to elevate your regulatory expertise? Our compact weekend study program is designed to help you master EU - MDR. Whether you are looking to level up your career, gain hands on regulatory skills, or you wanted to prepare confidently for regulatory credential exams, this program is the perfect fit!

SESSION DETAILS:

Start Date: May 10, 2025 
End Date: June 14, 2025
Mastery Session: June 15, 2025

   Registration closes by: May 08, 2025
   Timing - Every Saturday
9:30 AM to 11:30 AM (EDT)
Platform: Online - Microsoft Teams

ALL INCLUSIVE PRICE

CAD $75 ONLY

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.

Download the brochure for Program Breakdown

  • High Quality Lectures

  • 16 hours live Training

  • Access to training materials

  • 6 Quizzes - 20 questions each

  • 2 Practice Tests - 120 questions each

  • Live demos & real-world MDR scenarios

  • Hands-on EU-MDR Assignments

  • 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.

 What learners found most valuable?

Nakul Pathak

Batch - 02 (2024)

Nivedha’s deep understanding of EU-MDR was key to both the theoretical and practical aspects of the regulation. She not only answered my questions but also helped me understand some of the more detailed parts of the regulation that are often overlooked in other training. Nivedha has a great way of breaking down complex topics and making them easy to understand. Overall, I highly recommend Nivedha for anyone looking to learn about EU-MDR, whether for exams or professional certification. Her teaching style, expertise, and support with exam prep make her an outstanding trainer.

Srinithi
PMS specialist
Batch - 01 (2025)

Her in-depth knowledge and expertise in the field of regulatory affairs were evident throughout our collaboration. Her ability to break down complex regulations into understandable and actionable insights was impressive. Her professionalism, responsiveness to queries throughout the session were greatly appreciated. I highly recommend Nivedha to anyone seeking guidance on RCC MDR certification preparation

Arun Burra 
Licensed Pharmacy Tech
Batch -01 (2025)

Since I have no experience, it was great to hear about in-field experiences & examples that was relatable to the content & made learning much easier. I find the experience of Nivedha very valuable in presenting the content & helping the attendees meet their goals.The content was made understandable to people with different levels of experience, which I appreciated the most. I will be looking forward to more courses from her.

 Prabhu Muthu
Senior Lead - Regulatory Affairs 
Batch - 01 (2024)

Crisp and Clear information along with live examples and I felt like back to college days and learning things.

Fatemeh Rahimi
Quality & Regulatory Affairs Manager
Batch - 02 (2024)

Consistency of the sessions and participation of the people.

Angela Lema-PerezRegulatory Affairs Specialist
Batch - 01 (2025)

The most valuable of the sessions is PMS plan and report, Post Market Surveillance

 Barath Kumar
Regulatory Affairs Associate 
Batch - 01 (2024)

Consistency of the sessions and participation of the people. What I found most valuable about the session was the opportunity to connect with regulatory professionalsfrom various domains and regions. Sharing their regulatory knowledge and experiences was incrediblyhelpful. The in-depth review of regulations ensured that we didn't miss any critical information. Particularly,having a tricky quiz at the end of each session was really beneficial and helped test our regulatory knowledge.

Sai Prathyush Jogiparthi
Regulatory affairs specialist
Batch - 01 (2025)

Materials, interaction and knowledge sharing.

Lakshmi Channappa
Specialist medical devices technical writing
Batch - 01 (2025)

The content being well structured and well timed.

Gautamee Choudry
Thyagaraj Regulatory AffairsSpecialist - Consultant
Batch-01 (2025)

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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