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standard operating procedure for the direct antiglobulin test

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Provincial Blood<br />

Coordinating Program<br />

Standard Operating Procedure For<br />

Per<strong>for</strong>ming The Direct Antiglobulin<br />

Test.<br />

10.0 Records Management<br />

10.1 The recipient transfusion data file in <strong>the</strong> transfusion service laboratory shall<br />

be retained indefinitely.<br />

10.2 All transfusion records in <strong>the</strong> recipient’s medical chart, shall be retained in<br />

accordance with health care facility’s retention policy <strong>for</strong> medical records.<br />

10.3 Quality control of blood components, blood products, reagents and<br />

equipment shall be retained <strong>for</strong> 5 years.<br />

10.4 Date and time of specimen collection and phlebotomist’s identification shall<br />

be retained <strong>for</strong> 1 year.<br />

10.5 Request <strong>for</strong>m <strong>for</strong> serologic <strong>test</strong>s shall be retained <strong>for</strong> one month.<br />

10.6 Documentation of staff training and competency must be kept <strong>for</strong> a<br />

minimum of ten years.<br />

10.7 Refer to CSTM Standards, Appendix A and CSA Standards, Table 4 <strong>for</strong><br />

additional record retention requirements.<br />

_______________________________________________________________________<br />

This document may be incorporated into each Regional Policy/Procedure Manual.<br />

NL09-005<br />

Version: 2.0<br />

Effective Date: 2011-02-14<br />

Page 10 of 12

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