健康・人 · 薬局・ライフサイエンス

薬局・ライフサイエンス向けの AI アプリケーション

処方箋のわかりやすさの確認、調剤ラベルや服薬指示の作成、在庫と規制医薬品の記録の整備を行います。

これらのアプリケーションが担う業務

処方箋を確認

処方箋の不明確な点に印を付け、薬袋のラベルと患者が持ち帰る服薬指示を作成します。

わかりやすい説明書

患者向けの説明書をわかりやすい言葉で書き直し、服薬指示を患者の言語に翻訳します。

在庫を管理

欠品のお知らせを起案し、麻薬・向精神薬の記録簿の記載を構造化し、発注の優先順位を付けます。

この業種のアプリケーション

  • Prescription Clarity Check

    Lists every prescribed line field by field and flags what is missing or unclear before the pharmacist calls the prescriber.

  • Dispensing Label Writer

    Turns prescriber shorthand into one clear dosage instruction ready to print on the dispensing label.

  • Leaflet Plain Language

    Rewrites a pasted section of a patient information leaflet into wording a customer can actually read at the counter.

  • Patient Directions Translator

    Translates dispensing directions and safety warnings into the patient's language without altering a single number.

  • Stock Shortage Note

    Gives counter staff the exact words to explain an out-of-stock medicine and what happens next.

  • Controlled Drug Entry

    Converts a dispensing record into register-ready rows and names every mandatory field still missing.

  • Reorder Priority Ranker

    Ranks your stock lines by how urgently they need reordering before the next wholesaler cut-off.

  • Recall Action Planner

    Turns a batch recall notice plus your stock position into an ordered action plan for the responsible pharmacist.

  • Claim Rejection Resolver

    Explains a payer rejection message in plain language and lists the steps to get the claim paid.

  • Medicines Review Digest

    Structures a medicines use review into what the patient takes, what they said, and the questions left for the pharmacist.

  • Cold Chain Incident Note

    Writes the factual record of a fridge temperature excursion for the quality file, without deciding the stock's fate.

  • Adverse Event Intake

    Extracts the four case validity elements and every reportable field from a free-text side effect report.

  • Case Seriousness Triage

    Labels a safety case Serious or Non-serious against the regulatory criteria and quotes the phrase that decided it.

  • Medical Information Reply

    Drafts a reply to a healthcare professional enquiry that stays strictly inside the approved response content.

  • Deviation Record Writer

    Turns a shop-floor deviation note into a structured GMP deviation record ready for QA review.

  • Audit Finding Grader

    Grades a GMP or GDP audit observation as Critical, Major, Minor or Comment with a three-sentence justification.

  • Analysis Certificate Digest

    Reads a certificate of analysis and lists every parameter, its specification, and anything out of spec or absent.

  • Supplier Qualification Score

    Scores a supplier questionnaire out of 100 against your weighted criteria and returns an approval band.

  • Protocol Synopsis Brief

    Condenses a clinical trial synopsis into the six things a site team needs before the investigator meeting.

  • Screening Eligibility Checklist

    Converts inclusion and exclusion criteria into a numbered yes/no checklist a screener can work through.

  • Inhaler Technique Script

    Produces the step-by-step words to say while teaching a patient the device they were just handed.

  • Repeat Request Screener

    Sorts a batch of repeat prescription requests into ready to issue, needs pharmacist review, or query the patient.

  • Discharge Medicines Reconciliation

    Compares the admission and discharge medicine lists and returns every start, stop, dose change and unexplained difference.

  • Counter Enquiry Questions

    Gives counter staff the questions to ask before an over-the-counter request goes any further.

  • Clinical Intervention Log

    Turns a scribbled intervention note into a complete log entry with the fields your audit needs.

  • Compounding Worksheet Draft

    Lays out an extemporaneous formula as a worksheet with ingredients, method steps and the in-process checks to sign.

  • Antimicrobial Switch Review

    Structures an intravenous-to-oral antibiotic review into the criteria met, not met, and unknown for the ward round.

  • Artwork Text Comparison

    Lists every wording difference between carton or label artwork and the approved reference text.

  • Agency Question Reply

    Drafts the structured response to a regulator's question using only the assessment content you supply.

  • Approval Commitment Extract

    Pulls every post-approval commitment, condition and deadline out of an authorisation letter into a tracker list.

  • Change Impact Assessment

    Maps a proposed change to the documents, systems and approvals it touches before change control is raised.

  • Literature Case Screener

    Decides whether a published abstract contains a valid individual case report that must be processed.

  • Medication Error Classifier

    Labels a reported medication error by the stage it occurred at, whether it reached the patient, and the harm described.

  • Safety Case Narrative

    Writes the chronological case narrative for a safety report from the fields already collected.

  • Trial Consent Simplifier

    Rewrites a section of an informed consent form into wording a trial participant can actually understand.

  • Monitoring Visit Report

    Turns raw site visit notes into a structured monitoring report with findings and follow-up actions.

  • Data Clarification Query

    Writes the neutral query text sent to a site about a discrepancy in the trial database.

  • Lay Results Summary

    Condenses reported trial results into the plain-language summary participants and the public are owed.

  • Out Of Spec Investigation

    Opens a laboratory investigation into an out-of-specification result with the checks to perform in order.

  • Lab Notebook Entry

    Converts bench scribbles into a dated, auditable experiment record ready to be countersigned.

  • Reagent Safety Card

    Reduces a supplied safety data sheet extract to a one-page bench card for the people handling the reagent.

  • Corrective Action Plan

    Turns an agreed root cause into separate corrective and preventive actions with owners and verification steps.

  • Quality Complaint Router

    Separates a customer complaint into the product quality part, the safety part, and the questions still to ask.

  • Deviation Trend Themes

    Groups a period's deviation descriptions into recurring themes with counts, for the quality review meeting.

  • Technical Agreement Summary

    Reduces a quality or technical agreement to a who-does-what table plus the responsibilities left unassigned.

  • Field Interaction Record

    Converts scientific field notes into a compliant interaction record, flagging anything that needs review.

  • Promotional Claim Check

    Tests each claim in a promotional piece against the approved reference text and flags what has no support.

  • Congress Abstract Recap

    Compresses a congress abstract into the study, the result and the limitations a field team can repeat accurately.

  • Procedure Step Rewrite

    Rewrites a narrative procedure into numbered SOP steps with the role responsible for each one.

  • Batch Record Reconciler

    Returns a line-by-line list of the blank entries, out-of-range figures and unfinished steps found in an executed batch record.

  • Wholesaler Invoice Audit

    Returns the invoice lines that do not match your order: short supplies, price changes and items you never asked for.

  • Stability Trend Readout

    Turns a stability study timepoint table into a plain readout of which attributes are drifting towards specification.

  • Cleanroom Excursion Digest

    Summarises an environmental monitoring export into the excursions, the rooms involved and the points that were never sampled.

  • Formulary Update Brief

    Turns a formulary committee decision document into a short brief of what changed for prescribers and ward stock.

  • Tender Obligation Checklist

    Pulls every stated requirement, deadline and mandatory enclosure out of a tender pack into one numbered checklist.

  • Care Home Chart Review

    Reads a medication administration chart export and lists the gaps, coded rounds and repeat omissions that need chasing.

  • SOP Training Shortfalls

    Turns a training matrix spreadsheet into a per-person list of overdue, missing and undated SOP training.

  • Calibration Certificate Check

    Reads an equipment calibration certificate and returns the accept or reject verdict, the deviations found and the next due date.

  • Vaccine Schedule Extract

    Extracts from an immunisation protocol who is eligible, the product and dose, the intervals and the listed exclusions.

  • Carton Detail Transcriber

    Reads a photo of a medicine carton and returns the printed product details as typed, labelled fields.

  • Damaged Delivery Report

    Writes the condition report you send the wholesaler, from a photo of a damaged pharmacy delivery.

  • Instrument Display Log

    Turns a photo of an instrument display or printout into a typed log entry ready for the record.

  • Dispensary Tidy Audit

    Scores a photo of the dispensary bench against basic housekeeping standards and lists what to fix first.

  • Waste Segregation Check

    Classifies what is visible in a pharmaceutical waste bin photo and names anything sitting in the wrong stream.

アプリケーションの仕組み

業務を選ぶ

各アプリケーションは、その業種の業務を 1 つ担い、1 文で説明されています。

フィールドに入力

アプリケーションが求めるフィールドに、メモ、メッセージ、文書の抜粋を貼り付けます。

回答を活用

コピー、送信、保存できる構造化された結果を読むか、Ultineo AI の API から取得します。

これらの業務を Ultineo AI に任せる

チームに必要なアプリケーションをお知らせください。アクセスを開設します。

これらのアプリケーションに関するご質問

はい。各プランには、カスタマイズできるアプリケーションが一定数含まれており、フィールドや指示を自社のやり方に合わせられます。

フィールドで求められる内容だけです。たとえばメモ、メッセージ、文書の抜粋などです。業務に必要な範囲を超えて個人データを共有しないでください。

はい。Ultineo AI の API は、プロジェクトで利用できるすべてのアプリケーションを起動し、実行が完了すると回答を返します。