Regulatory Augmented Intelligence 5.0 introduces significant enhancements to its chatbot suite, including incremental info updates, a notification feature for completed responses, and a new thinking effort slider for processing complexity. Free users now access high-level AI capabilities, while the Prompt Library offers templates to ease user inquiries, improving overall interaction efficiency.
Prompt library The new Prompt Library in the Regulatory Augmented Intelligence (RAI) tools is a bit like walking into a meeting with the agenda already written. Instead of staring at a blank chat window wondering how to begin—what do I say to ChatMDR, or how do I phrase this for ChatFDA?—you now get a curated …
ChatMDR July 2025 update New MDCG and FDA guidances came out, so it is time for the quarterly update of everyone’s favourite RA chatbots. Here’s what’s been included as of July 14, 2025: ChatMDR ChatIVDR ChatAIAct ChatFDA On average, the AI tools are updated with new guidances once every three months – of course depending …
Introducing RAI Enterprise ChatMDR, ChatIVDR, ChatFDA and since recently, ChatAIAct have been the domain of pioneering regulatory professionals. In the past year and a half, the tools have grown from a novelty to an essential part of the regulatory toolbox. Now comes the time to implement Regulatory Augmented Intelligence in organisations at large. This is …
(Always) keeping your data safe As a user of ChatMDR, ChatIVDR or ChatFDA, you know that one of the key promises of these tools is that they keep your data safe. Your inputs and outputs are not shared with anyone. They are not used for model training. Why is using data for model training dangerous? …
Pricing There are three ways to enjoy Regulatory Augmented Intelligence with ChatMDR. The first one is that ChatMDR, ChatIVDR, ChatAIAct and ChatFDA have free entry tier. It is our intention to let it always be free. We want to have a low barrier to entry for people who just want to try our tools. If …
FDA Classification FDA Classification is a tool that augments ChatFDA with one very specific function: finding the device class for a medical device and possible equivalent devices in the FDA’s 510(k) database. How to use You find FDA Classification in the dropdown menu, right under ChatFDA. The input to FDA Classification is as much information …
FDA Classification and other enhancements in ChatFDA / ChatMDR 3.3 The latest release of our regulatory AI suite brings some interesting enhancements. A whole new feature aimed at devices under the 510(k) substantial equivalence schemes and functionality enhancement for all tools, whether you’re looking at Europe or the US and at medical devices or in-vitro …
ChatFDA is ChatMDR for the FDA medical device regulation in the United States. It is an AI chatbot intended to help you with 510(k) and PMA processes with the FDA. It was released in December 2024.
ChatMDR 3.1 was launched in October 2024, featuring the new GPT o1 model. This revision emphasizes advanced reasoning skills and problem-solving capabilities. Three models are supported: Fast, Smart, and Reasoning. The Reasoning model excels in analyzing complex problems step-by-step, utilizing innovative strategies like chain-of-thought reasoning to enhance accuracy.
