A licensee shall ensure that a test report includes but is not limited to the following: Name and physical address of the laboratory; A unique identifier on each page of the report; Identification of the forensic analysis method used; A clear identification of each item tested including a description of the item’s condition; The date each forensic analysis was completed; Units of measurement, if applicable; The name and written or electronic signature of the examiner or analyst responsible for: Performance of the forensic analysis; Interpretations of forensic analysis results; and Opinions; Opinions and interpretations; When applicable, a statement of uncertainty of measurement if the uncertainty of measurement may affect the interpretation of the results of the forensic analysis; The date report was generated; The indication of the end of the report on the report’s last page; and If applicable, a statement that the analysis was performed by another laboratory and identifies the facility that actually performed the analysis. A licensee shall ensure that any information from §A(1)—(12) of this regulation that is not included in the test report is documented in the case record. A licensee shall ensure that test reports: Are produced when analytical testing is performed on evidence; Contain opinions and conclusions and the name of the report’s author; Report results accurately, clearly, unambiguously, and objectively; and Utilize a page numbering system that includes either the total number of pages or a mark to signify the end of the document. A licensee shall ensure that amended reports: Clearly state that the report has been amended; Reference the original report; Are placed or associated with the original report in the case file; and Are provided to the customers. Reports — Postmortem Forensic Toxicology. In addition to applicable sections of this regulation, a laboratory performing postmortem forensic toxicology shall: Have a procedure or policy for technical review of reports, which includes at a minimum: Chain of custody documentation; Validity of analytical data; and Quality control data; Include on the test report the name of the submitting agency or individual; Indicate qualitative test results using the: Term “Positive” if the test result is positive for the presence of the substance tested; and Term “None detected” if the test result is negative for the presence of the substance tested; Have quantitative results identified using correct nomenclature; Have preliminary reports clearly indicate that the: Results are unconfirmed and subject to verification; Testing is incomplete; and Subsequent results, where appropriate, may affect the final report and interpretation of the report; Clearly identify test results performed by a subcontractor; Clearly identify revised reports or addenda using the same identifying information as the original report, for reports that contain additional testing after the original test results were reported; and Indicate on the final report the name of the laboratory that actually performed the test if specimens were referred to another laboratory for analysis.