Specifications include, but are not limited to: Task 1: Perform initial assessment of the status of the laboratory’s management system documentation. This should include review of the quality assurance plan (QAP) and other associated quality management documents, laboratory standard operating procedures (SOP) for the accredited methods/analytes, instrument/method validation data, and demonstration of capability (DOC) certificates from the analyst(s) performing the various analytical methods. A list of the accredited methods/analytes is provided in this document (Attachment H). Preliminary evaluation shall be in narrative format to be delivered no later than fourteen (14) ten calendar days after the document review is completed. Results of the preliminary evaluation can be included in the final report, as needed.