Section R. 325.9083 - Reporting responsibilitiesRule 3.
(1) All clinical laboratories and users of portable blood lead analyzers doing business in this state that analyze blood samples for lead shall report all blood lead results for adults and children to the department electronically consistent with rule (4). If a result and required reportable information under rule (2) cannot be reported electronically within the time frame specified by this rule, then the results must be submitted to the Michigan Department of Health and Human Services, Childhood Lead Poisoning Prevention Program (CLPPP), P.O. Box 30037, Lansing, MI 48909, or by fax to (517) 335-8509. Reports must be made to the department within 5 working days after test completion. Nothing in these rules prevents a person or entity required to report under these rules from reporting results to the department sooner than 5 working days.(2) Nothing in this rule relieves a clinical laboratory or a user of a portable blood lead analyzer from reporting results of a blood lead analysis to the physician or other health care provider who ordered the test or to any other entity as required by state, federal, or local statutes or regulations or in accordance with accepted standard of practice, except that reporting in compliance with this rule satisfies the blood lead reporting requirements of section 5474(1)(c) of the public health code, 1978 PA 368, MCL 333.5474.Mich. Admin. Code R. 325.9083
1997 AACS; 2015 AACS; 2020 MR 3, Eff. 2/7/2020