Conversational guide to EU MDR, IVDR, and MDCG guidance documents, with clear, bullet-pointed answers.
π¬ 4+ Chats
Use This GPTGuides on AI healthcare device compliance with EU MDR, using uploaded documents.
π¬ 5+ Chats
Expert on IVDR, providing guidance and clarifications on regulatory topics.
π¬ 6+ Chats
Experte fΓΌr IVDR, bietet detaillierte und genaue regulatorische Informationen.
π¬ 3+ Chats
Expert in EU medical device registration, offering downlink to download regulation documents and guidance on MDR
π¬ 50+ Chats
Assistant for product classification according to EU MDR 2017/745.
π¬ 70+ Chats
Suggests the correct MDR classification for your medical device based on the MDR Annex VIII Classification Rules. Please provide a description of your...
π¬ 10+ Chats
A conversational AI assistant developed to help navigate data and answer questions related to the Office of the Conflict of Interest and Ethics Commissioner...
π¬ 10+ Chats