CQC Medicines Optimisation

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CQC Medicines Optimisation

To provide an outline of the evidence for CQC Medicines Optimisation (MO) requirements and support to enable practices to meet the CQC inspection requirements. 

This will cover:

  • Responsibilities and accountabilities 
  • Policies and processes 
  • High risk medicine monitoring  
  • Medicines safety: Acting on safety alerts 
  • Long term condition management 
  • Medication Reviews  
  • Clinical supervision  

Sessions

CQC Medicines Optimisation — Afternoon

Friday, 10th November 2023 / 1.00pm

See above.

 

https://teams.microsoft.com/l/meetup-join/19%3ameeting_MGQ0MjUyMDEtNjFhYi00ZjBlLTllYjctOWJhNzRhMmEyY2Fi%40thread.v2/0?context=%7b%22Tid%22%3a%2237c354b2-85b0-47f5-b222-07b48d774ee3%22%2c%22Oid%22%3a%2209430d52-b4d4-40e8-8ca0-517941ce99b0%22%7d