Practice information required for this page
Upcoming Changes
These changes will be rolled out in February 2026.
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New or updated pages
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What's changing?
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What do you need to do?
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Draft: Adverse Events
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- This policy has been updated to align with the National Adverse Events Policy 2023 and recent RNZCGP guidance on adverse events. Definitions and processes have been updated to align with HQSC requirements.
- Adverse reactions are now reported via the national pharmacovigilance database, a joint system managed by Medsafe and CARM.
- Management of SAC 1 and 2 events to HQSC is via the national reporting tool within specified timeframes.
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Draft: Open Disclosure
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- This policy has been updated to align with the National Adverse Events Policy 2023 and recent RNZCGP guidance on adverse event management in general practice.
- Definitions have been updated and processes changed so that the policy follows a relational approach to disclosing events, with a focus on restoring trust.
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Draft: Medical Equipment
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- Policy updated to reflect recent guidance from RNZCGP.
- From February 2026, practices who don't have a body protected area need to install one, or put a plan in place for transitioning to one.
- More information added about body protected areas and residual current devices including expanded explanations of the requirements for BPAs, and the requirements for installation, inspection, servicing and compliance.
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Pages to be retired
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Why?
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There are no pages being retired this month.
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