Module 1 - Study of Errors Module 2 - Event Reporting Module 3 - MERS-TM Glossary Training Introduction
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It was determined that event reporting should be included as part of Quality Assurance (QA) efforts in transfusion medicine for two main reasons.

  1. QA is already required by regulation and a duplicate system would be resisted.

  2. The MERS-TM system should be compatible with established QA standards of blood bank organizations such as the AABB and Federal regulations from the FDA.

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