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bhunterlabguy

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Everything posted by bhunterlabguy

  1. Problematic - Since the CLIA director responsibilities do not allow this set of duties to be delegated, the CLIA director must be available 24 x 7 x 365. The CLIA prosgram only appllies to patient testing. If CAP requires all polices, etc. to be annually signed by the CLIA director, then it would be an accreditation requirement.
  2. Just and FYI for those in CA. - For unlicensed staff - see Ca. Business and Professions code 1269 (d) (3) - For MLT's - see CBPC 1260.3 (. http://www.leginfo.ca.gov/cgi-bin/displaycode?section=bpc&group=01001-02000&file=1260-1275
  3. This "signing" only applies to patient test procedures, not other policies, procedues or processes, and is currently a hotly debated topic...
  4. I hate to be lame, but you could "Google" it. There are a number of vendors who supply kits and equipment for this process. There have been three facilities actually inquiring about licensing for this...
  5. Check AABB Stds also, p. 30, 27th ed. HBsAg, anti-HBc, Anti HCV, Anti-HIV 1/2, and anti-HTLV I/II still required.
  6. I have read the threads and have seen many of those situations. Perhaps it is time to go for the money. If your accrediting (or regulatory) agency knew about these non-compliance issues, serious deficiencies and/or out-of-cycle visits might get the attention of those "above".
  7. Here is a link you can use... http://www.cdc.gov/nhsn/bio.html
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