Rule 16.02.06 - QUALITY ASSURANCE FOR CLINICAL LABORATORIES
- Section 16.02.06.000 - LEGAL AUTHORITY
- Section 16.02.06.001. - 009 - RESERVED
- Section 16.02.06.010 - DEFINITIONS
- Section 16.02.06.011. - 099 - RESERVED
- Section 16.02.06.100 - REGISTRATION REQUIREMENTS
- Section 16.02.06.101. - 109 - RESERVED
- Section 16.02.06.110 - EXCLUSIONS
- Section 16.02.06.111. - 119 - RESERVED
- Section 16.02.06.120 - DEPARTMENT INSPECTIONS
- Section 16.02.06.121. - 129 - RESERVED
- Section 16.02.06.130 - GENERAL REQUIREMENTS
- Section 16.02.06.131. - 149 - RESERVED
- Section 16.02.06.150 - PERSONNEL REQUIREMENTS
- Section 16.02.06.151. - 199 - RESERVED
- Section 16.02.06.200 - PROFICIENCY TESTING
- Section 16.02.06.201. - 209 - RESERVED
- Section 16.02.06.210 - QUALITY CONTROL PROGRAM REQUIREMENTS
- Section 16.02.06.211. - 219 - RESERVED
- Section 16.02.06.220 - DEPARTMENT APPROVAL
- Section 16.02.06.221. - 229 - RESERVED
- Section 16.02.06.230 - DEPARTMENT REVOCATION OF APPROVAL
- Section 16.02.06.231. - 239 - RESERVED
- Section 16.02.06.240 - REVOCATION PROCEDURE
- Section 16.02.06.241. - 249 - RESERVED
- Section 16.02.06.250 - RENEWAL OF APPROVAL OF DISAPPROVED TEST(S)
- Section 16.02.06.251. - 269 - RESERVED
- Section 16.02.06.270 - REGISTERED LABORATORIES
- Section 16.02.06.271. - 299 - RESERVED
- Section 16.02.06.300 - FAILURE TO REGISTER OR OPERATION OF AN UNREGISTERED CLINICAL LABORATORY
- Section 16.02.06.301. - 999 - RESERVED