Common Assessment Requests

In-store assessment

The move back to in-store assessments means that you need everything to be current, available and readily accessible. The assessor may ask for any piece of evidence listed in the QCPP Requirements.

These are common requests that we have heard about in recent assessments:


Domain 1

  • Written business plan

  • Risk management plan

  • Signed attestation statement

  • Business governance agreements – signed by owners and all staff pharmacists

  • Pharmacist self-assessment and professional indemnity insurances

  • Business insurances – professional indemnity, public liability, workers compensation

  • Policy annual review evidence

  • Incident reports and register

  • Quality improvement process and register


Domain 2

  • Privacy and Confidentiality policies signed by all staff – or evidenced in their induction – that they will maintain consumer privacy and confidentiality.


Domain 3

  • Staff files each contain:

    • Position description

    • Contract of employment

    • Induction checklist

    • S2S3 training certificate for new staff and Refresher Training records for existing staff

    • Performance reviews

    • Training plans and records (inc S2S3 above) 


Domain 4

  • Active monitoring of fridge temperatures – twice daily recordings and loggers with alarms and warning system, if fridge goes out of range

  • Cytotoxic medicines are labelled as such in the dispensary

  • Position of S2 and S3 stock is as per State or Territory requirements

  • Pseudoephedrine products are position so that they are not accessible to consumers, are out of sight of consumers and have single facings

  • Recalled, damaged and out-of-date stock is quarantined appropriately

  • Show that at least one staff member has current First Aid and CPR training at all times the pharmacy is open


Domain 5 

  • Records of Dispensary Incidents and evidence/proof that these have been investigated and when necessary actioned to resolve and prevent re-occurrence, as shown in the Quality Improvement Register

  • Complex compounding risk management plan and mitigation activities.

  • Complex compounding final products are tested and verified independently

  • Complex compounding certificate of training by all staff involved, from either PCCA or Medisca

  • Service recording system and evidence e.g. patient’s leave certificate

  • Service recording system and evidence of a disease state management service (e.g. BP check) and a screening and risk assessment service (e.g. BP check)

  • All professional services - training evidence for staff involved in the service

  • Staged supply and ORT service agreements and signed records for each provision

  • Details of training by all staff who have access to MHR

  • MHR security and access policy signed by all staff – could be on the policy itself or evidenced by the staff induction checklist


What to do now

Get up to date (check Recent Updates) and then, using Pharmacy Hive, maintain all required evidence recording and storing as it happens, so that next assessment is stress-free because everything is ready to go, all the time!

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