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 …
ChatMDR 4 models explained As of ChatMDR, ChatIVDR, ChatFDA and ChatAIAct version 4 (April 30, 2025) there are three different AI models available, each with their own characteristics. Here’s how to make the most of each. First of all, the obvious: how to select each model. This is done using the model selector, which 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 …
o3-mini is the new Diamond Experienced ChatMDR, ChatIVDR or ChatFDA users know that Diamond is synonymous with the smartest model of them all. It takes a bit of time to break a complex problem down into steps and then not only solve the problem, but also explain its reasoning. This makes the output verifiable and …
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 …
Account creation and subscription Here’s a quick video that shows how to create a ChatMDR account from scratch, upgrade your subscription to ChatMDR Plus and also cancel your subscription without any further cost. Also, it highlights the entry of a discount code, such as those given out to select customers. Interested in a free trial …
Prompting guide Getting better answers from AI Have you ever tried using ChatMDR or ChatFDA, only to wonder if you were missing something? One key to getting the best outcome is a method known as “prompting.” This approach shapes how we communicate our requests to these powerful systems. Prompting is telling the AI model what …
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.
