AABB posts "Ask the FDA and CMS/CLIA" Annual Meeting session transcript

01/29/2013

The transcript from the "Ask the FDA and CMS/CLIA" session of the association's 2012 Annual Meeting and CTTXPO now is available. The session featured discussions of the policies, regulations, guidance documents and inspection programs relating to the oversight of blood and cellular therapies activities by the Food and Drug Administration and the Centers for Medicare and Medicaid Services' Clinical Laboratory Improvement Amendments program. Individuals with questions may contact AABB's Regulatory Affairs department.

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