Prompt
Draft a High-Alert Medication Policy
Use this when you want to create or update a policy for handling high-alert medications in your pharmacy.
How to use it
- Copy the prompt and paste it into ChatGPT, Claude, Gemini or any other AI.
- Replace every {{placeholder}} with your own details, or let the AI ask you for them.
- Use the follow-ups below to go deeper.
Role You are a pharmacy policy writer supporting a pharmacist-in-charge. You produce a high-alert medication policy that staff can follow at the bench and an inspector can audit line by line.
Context you provide
- {{pharmacy_name_and_site_type}} — site and setting, e.g. community retail, hospital inpatient
- {{jurisdiction_and_regulator}} — country or state and inspecting body
- {{high_alert_medication_list}} — drugs or classes in scope
- {{existing_policy_or_gaps}} — current text or what is missing
- {{storage_and_verification_workflow}} — storage, labelling, order review, double checks
- {{staff_roles_and_training}} — who dispenses, who verifies, training frequency
- {{incident_and_audit_history}} — near misses, errors, last audit findings
- {{mandated_sections}} — headings your regulator requires
Instructions
- Ask for any missing inputs, then wait before drafting.
- Confirm the high-alert list and flag any entry that is a class, not a named medicine.
- Draft sections: purpose, scope, medicine list, procurement and storage, order review, dispensing and verification, counselling, monitoring, incident reporting, training, review cycle.
- For each control, state who performs it, when, and what evidence is recorded; add a table mapping each medicine to its safeguards.
- Mark points that depend on local regulation or manufacturer labelling with a check note.
- Close with an implementation checklist and a review date placeholder.
Output format Markdown policy, 900 to 1,400 words, numbered clauses, tables for the medicine list and safeguards, plain professional tone. No invented drug names, thresholds or regulation numbers. Leave out marketing language and general medication safety theory.
Guardrails
- Do not invent drug names, dose limits, storage temperatures or regulation citations; use only what I provide or mark as [to confirm].
- Flag every assumption and every point where the local regulator or a manufacturer's labelling must be checked before sign-off.
- Do not present the draft as legal or accreditation advice.
Example Pharmacy: Riverside Community Pharmacy, community retail; regulator: state board of pharmacy; high-alert list: insulin, anticoagulants, methotrexate, opioids.