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CQC controlled-drugs & stock audit checklist

A practical checklist to help UK clinics, GP surgeries and private practices keep controlled-drug registers, stock and expiry records inspection-ready. Work through it as a self-audit, or use it to brief your team before a review.

General guidance to support good record-keeping - not legal or regulatory advice. Always follow your own policies and current CQC, MHRA and Misuse of Drugs Regulations requirements.

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The checklist

Controlled-drug register

  • A bound or tamper-evident CD register (or a validated electronic equivalent) is in use for each Schedule 2 (and relevant Schedule 3) drug.
  • Every entry records date, drug, form and strength, quantity received or supplied, running balance, and the person responsible.
  • Receipts and administrations are witnessed and signed where your policy requires it.
  • Running balances are reconciled against physical stock on a defined schedule (e.g. weekly), and discrepancies are investigated and recorded.
  • CD stock is held in an appropriate, access-controlled cabinet, with a documented key/access holder.
  • Expired or returned CDs are destroyed/denatured following the correct procedure, with a witnessed record.

General stock & medicines management

  • A current list of all medicines and consumables held, with agreed minimum/maximum levels.
  • Stock is stored correctly (temperature, security, segregation) and fridge temperatures are logged where relevant.
  • Receipt of stock is checked and recorded against orders.
  • A named person is accountable for ordering, receipt and stock control.
  • Usage is recorded so stock levels reflect reality between counts.

Expiry & waste

  • Expiry dates are checked on a defined schedule and near-expiry items are flagged in advance.
  • Out-of-date stock is removed from use promptly and disposed of correctly, with a record.
  • Wastage is recorded and reviewed to reduce avoidable loss.

Audit trail & inspection evidence

  • Every stock movement can be traced to who did what and when.
  • Records can be produced quickly on request (register, reconciliations, temperature logs, destruction records).
  • Standard operating procedures for medicines and CD management are documented, in date, and staff have read them.
  • Access to records and stock is limited to authorised staff, and access is auditable.
  • A recent internal audit / spot-check has been carried out and any actions closed off.

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