chatfda

FDA Classification released – version 3.3

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 …

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Maarten explaining something

Prompting guide

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 …

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