Sec. 20531.
Not later than 90 days after the effective date of this section, the department shall mail a notice to each clinical laboratory doing business in this state explaining the reporting requirements of this section. Beginning October 1, 2005, a clinical laboratory that analyzes a blood sample for lead shall report the results of the blood lead analysis to the department electronically in a format as prescribed by the department. The clinical laboratory shall submit the report to the department as required under this section within 5 days after the analysis is completed.
History: Add. 2004, Act 54, Imd. Eff. Apr. 12, 2004 Popular Name: Act 368
Structure Michigan Compiled Laws
Act 368 of 1978 - Public Health Code (333.1101 - 333.25211)
Article 17 - Facilities and Agencies (333.20101...333.22260)
368-1978-17-205 - Part 205 Clinical and Other Laboratories (333.20501...333.20554)
Section 333.20501 - "Laboratory" Defined; Principles of Construction.
Section 333.20507 - Laboratories to Which MCL 333.20501 to 333.20525 Inapplicable.
Section 333.20511 - Repealed. 2015, Act 104, Eff. Oct. 1, 2015.
Section 333.20515 - Repealed. 2015, Act 104, Eff. Oct. 1, 2015.
Section 333.20525 - Repealed. 2015, Act 104, Eff. Oct. 1, 2015.
Section 333.20531 - Lead Analysis; Clinical Laboratory Reporting Requirements.