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STAT+: AI health care companies say they’ll keep humans in the loop. But what does that actually mean?

STAT

A flurry of AI-guided ambient documentation startups can rapidly transcribe and summarize patient visits and populate patients’ medical charts, but they require doctors and nurses to OK the generated entries first.

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Medical Documentation

RX Note

In addition, medical records are used in the management and planning of health care facilities and services, for medical research and the production of health care statistics. Since we don't even remember what we eat this morning, it is vital to make proper medical documentation.

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UK gov’t defends NHS data sharing plans in strategy document

pharmaphorum

The UK’s Department of Health and Social Care has published a document setting out its strategy on handling patient data – and defending its plan to transfer millions of GP records into a centralised database. The post UK gov’t defends NHS data sharing plans in strategy document appeared first on.

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Confidentiality

RX Note

Ensure no unauthorized personnel can gain access to patient medication records (e.g. Do not dispose of confidential documents and other media-containing sensitive information with regular waste. If talking about your work to family or friends, only talk about patients in very general terms.

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Episode 918: What Happens If You Give a Cephalosporin to a Patient With Moderate, Severe, or Unknown Beta-Lactam Allergy?

Pharmacy Joe

Subscribe on iTunes , Android , or Stitcher The label of “penicillin allergic” usually sticks to a patient’s medical record forever. The trouble is that many recorded allergies are actually intolerances, such as nausea, vomiting, and diarrhea.

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NHS data sharing scheme “on hold” as millions opt out

pharmaphorum

The centralised database of medical records from 55 million people was first unveiled in May and due to come online on 1 July, but had its start date pushed back to 1 September after campaigners pushed back against the proposals. million in June – and a drive should be carried out to raise awareness of the scheme.

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Lots of FDA Guidance, But Few Drug Manufacturing “Remote Interactive Evaluations” (We Would Call Them “Virtual Inspections”)

FDA Law Blog: Biosimilars

Admittedly, BiMo inspections (into items like adequacy of bioequivalence data, consistency of clinical trial data with medical records, and compliance with clinical trial protocols) lend themselves better to an RIE than assessing manufacturing compliance with regulatory requirements. We should explain what RIEs are.