Let's take reporting seriously
Reporting is not just ‘red tape’ – it is an essential part of clinical governance. Why? Because unless we observe and assess care outcomes and experiences on an ongoing basis - which reporting enables – we cannot effectively identify risks, emerging risks, or areas for improvement.
One example is reporting an adverse event following immunisation (AEFI), which is broadly defined as ‘any negative reaction that follows immunisation.’ By reporting an AEFI, it enables the Therapeutics Good Administration to:
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