79.00 CHF / month with a 5-day free trial
Navigating the maze of medical device regulations has never been easier, thanks to the Regulatory Affairs Expert Chatbot. Powered by the latest AI technology – ChatGPT-4, this groundbreaking tool is your 24/7 guide to the European regulatory landscape for medical and in-vitro diagnostic devices, providing instant, and evidence-backed responses to your inquiries with all the actual data related to EU Medical Device space.
Specialized Knowledge: Our chatbot is specifically trained in the European medical device field and has in-depth knowledge of key regulations like EU MDR 2017/745, EU IVDR 2017/746, MDSAP, ISO 13485, and all the actual data from today. This sets it apart from standard ChatGPT, which has general knowledge and is limited by September 2021.
Evidence-Backed Responses: Unlike the standard ChatGPT, our chatbot provides resources with every response, allowing you to see the evidence of the information shared and reinforcing your understanding.
24/7 Availability: Our chatbot is always on and ready to assist, providing instant responses to your queries at any time of the day or night.
Regular Updates: We regularly update the chatbot’s knowledge base with the latest regulatory changes, ensuring you always have access to the most current information.
Time and Effort Savings: The specialized knowledge and immediate responses provided by our chatbot can save you significant time and effort compared to searching for information yourself or using a general-purpose chatbot like standard ChatGPT.
Being always up to date with new or updated standards can be very time-consuming. That is where our standard tracking tool can help you. The tool tracks all ISO, IEC, IEEE, and DIN standards which are related to medical or in-vitro diagnostic devices.
Efficiency: Instead of manually checking various websites you have them all in one place.
Additional: You also can download all updates via an Excel list and use them for your own specific needs.
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