DR. INFO answers clinical questions from peer reviewed literature, current guidelines and FDA and EMA sources, with citations you can check against the original. These pages compare that against the tools European clinicians are weighing up, and every claim carries a numbered source.
Whichever tool you land on, these are the checks worth running before it reaches a patient.
Regulatory status decides this before features do. In the EU that means CE marking under EU MDR, GDPR compliant hosting, and a data protection officer who can sign it off.
Use real cases from your specialty, in the language you work in. General demos hide the gaps that matter to you.
Open the sources behind an answer. Check the reference exists, says what the answer claims, and applies to your patient.
A tool that says it does not know is safer than one that always produces a confident answer.
Ask who ran the evaluation, on what data, and whether the test resembles clinical work. A number without methods is marketing.