EU MDR and IVDR ChatBot

EU MDR and IVDR ChatBot

Getting started is as simple as typing your question into the chat interface. Whether you’re seeking clarity on a specific regulation like EU MDR or you need guidance on a broader topic like MDSAP, just ask away. Our ChatBot, powered by the latest AI technology is here to help with instant and evidence-backed responses.

Give us helpful feedback by completing the following survey.

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To make the most out of our ChatBot:

  • Be Specific: The more specific your question, the more precise the answer can be. Don’t hesitate to provide context or details like specific regulations or guidance.
  • Use Clear Language: For the best results, try to ask your questions in clear and concise language (English recommended).
  • Explore Topics: Don’t limit yourself to one topic. Our ChatBot is trained on a wide range of regulatory affairs subjects in Europe, so feel free to explore!
  • Review Attached Resources: With every response, our ChatBot provides resources that back up the information shared. Be sure to review these to deepen your understanding.


Remember, the ChatBot is a tool designed to guide and inform you, but for final decisions or complex situations, please use your experience as a Regulatory Affairs Professional or consult with a Regulatory Affairs Expert.

Disclaimer: This ChatBot is designed to provide information on European laws, regulations, and guidelines related to medical and in-vitro diagnostic devices. While we strive to provide accurate and up-to-date information, Regulatory Globe does not guarantee the accuracy, completeness, or applicability of any information provided by the ChatBot. The information provided by the ChatBot is not intended to replace professional advice. It is always recommended to consult with a Regulatory Affairs Expert or Professional for specific advice related to your particular circumstances. Regulatory Globe shall not be held responsible for any decisions made or actions taken based on the information provided by the ChatBot.