Complete AI Training

Prompt

Draft A Clinician Feedback Survey

Use this when you want to collect structured input on a device from healthcare staff in a consistent way.

How to use it

  1. Copy the prompt and paste it into ChatGPT, Claude, Gemini or any other AI.
  2. Replace every {{placeholder}} with your own details, or let the AI ask you for them.
  3. Use the follow-ups below to go deeper.
Prompt

Role You are a biomedical engineer drafting a clinician feedback survey about a medical device or system. You optimise for neutral, comparable questions that produce actionable engineering input.

Context you provide

  • {{device_name}} — device or system under review
  • {{clinical_area}} — ward, theatre, ICU, clinic or lab
  • {{feedback_goal}} — what you need to learn or decide
  • {{respondent_role}} — nurses, doctors, technicians, porters
  • {{survey_length}} — target question count or minutes
  • {{deployment_method}} — paper, online form, kiosk or email link
  • {{known_issues}} — complaints or incidents already reported
  • {{anonymity_rules}} — whether responses are anonymous
  • {{deadline}} — when responses are needed

Instructions

  1. Ask for any missing inputs, then restate the survey goal in one sentence for confirmation.
  2. Draft a short introduction covering purpose, who sees results, and completion time.
  3. Group questions into blocks: current use, usability, safety concerns, training, improvement ideas.
  4. Mix rating scales, single choice, and two or three open questions, worded neutrally.
  5. Include one question that lets a respondent flag a safety or patient risk immediately.
  6. Close with a thank-you and a route for urgent concerns, then list all questions in order with the response type beside each.

Output format Markdown with headings: Introduction, Questions, Closing. Number the questions and put the response type in brackets after each. Stay within {{survey_length}}. Plain professional tone. Leave out marketing language, device specifications you were not given, and promises about what will change.

Guardrails

  • Do not invent device specifications, incident data, regulatory references or standards numbers.
  • Flag any assumption about clinical workflow and ask the user to confirm it.
  • Tell the user to check local privacy, ethics and information governance rules before distributing, and to route patient safety concerns through the correct reporting channel.

Example Device: infusion pump; area: oncology day unit; goal: prioritise fixes for alarm fatigue; respondents: nurses; length: 12 questions; method: online form.