Selection of Reference Laboratories
Reference laboratories are chosen based upon quality of performance. Specimens must be referred only to a CLIA-certified laboratory or a laboratory meeting equivalent requirements as determined by Center for Medicare and Medicaid Services (CMS). Therefore, all requests for and approval of reference laboratories are required by the CLIA Laboratory Directors of UnityPoint Health - Des Moines Clinical Laboratories and Pathology Laboratory.
The Clinical Laboratory has a process for evaluating new test requests and qualifying reference laboratories to ensure quality of patient care, as well as compliance with accreditation requirements and applicable State/Federal laws including, but not limited to, possession of CLIA certification. New test requests will also be reviewed by the Laboratory Directors and Executive Director for medical necessity, consensus among applicable ordering providers, and cost and reimbursement. The review process for a new reference laboratory (send out test) may take approximately 8-10 weeks. Avoid collecting the specimen until the request has been approved unless previously discussed with the CLIA Laboratory Director (DM-Hospitals: Dr. Larry Anderson, MD or Pathology Laboratory: Dr. Jacob Sramek, MD).
Please contact the Kim Von Ahsen, Laboratory Quality & Safety Specialist at kimberly.vonahsen@unitypoint.org if you have any questions or concerns. Thank you!