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Medical Device EU

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Discovers all relevant guidances, regulations, and requirements in the European Medical Devices field.

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August 14, 2023
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Description

Generated by ChatGPT

Medical Device EU is a ChatGPT plugin that focuses on European Regulation in the medical device sector. It provides comprehensive information and assistance related to Medical Device Regulation (MDR), In Vitro Diagnostic Regulation (IVDR), compliance, classification rules, standards, and much more. This plugin is designed to simplify the regulatory landscape in medical devices, offering expertise in various aspects of medical regulatory affairs. |||

How to use:

1. Installation:

Users can either install the Medical Device EU plugin by searching for it in the ChatGPT plugin store or simply press the "try it" button at the top right of this page to open a chat in ChatGPT with the plugin already activated. |||

2. Querying Regulations:

To inquire about specific regulations such as MDR 2017/745 or IVDR 2017/746, users can simply type their questions in the chat. The plugin will provide detailed information about the selected regulation. |||

3. Classification and Standards:

Users can ask about risk classes, classification rules, ISO standards, and other related topics. The plugin will guide users through the relevant information and requirements. |||

4. Prompt Examples:

Here are some specific examples that users can utilize to interact with the plugin:

  • "Tell me about MDR 2017/745."
  • "What are the classification rules for medical devices?"
  • "Explain the transition provisions for MDR."
  • "Provide information about ISO 13485." |||

5. Subscribing to Newsletter:

For regular updates and news related to medical devices, users can subscribe to the newsletter at Regulatory Globe. |||

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Medical advice, Legal Advice, Product research
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