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MDR – language requirements for manufacturers (January 2024).xlsx

Excel document containing the language requirements for manufacturers under the Medical Device Regulation (MDR)-January 2024.

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March 24, 2024

ChatMDR interview: ChatGPT for the EU Medical Device Regulation. An interview between the creators.

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March 24, 2024

📅 MDR Transitional Provision Timeline

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Surveillance Agreement

Our AI Consultant Axel Explains the Legacy Device Surveillance Agreement!

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March 24, 2024

🚀 Three Essential Steps for Manufacturers to Extend MDD Certificates 🚀 1️⃣ Create a Regulatory Strategy and Timeline: Develop a comprehensive regulatory strategy, including timeline for the submission of your files for MDR conformity assessment. 2️⃣ Establish a MDR-Compliant QMS by May 2024: Implement a Medical Device Regulation (MDR) compliant Quality Management System (QMS) to…

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The Significance of the EU AI Act for Medical Devices

MDRChats-Available on spotify

MDR – language requirements for manufacturers (January 2024).xlsx

ChatMDR interview: ChatGPT for the EU Medical Device Regulation. An interview between the creators.

ChatMDR-AI for MDR

CHATMDR

CREATE’s birthday-3rd year

📅 MDR Transitional Provision Timeline

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