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c. Any other documentation and reports associated with work performed for this contract shall be <br /> likewise retained and shall include relevant information for the procedures described in sections 2 <br /> and 3,above. <br /> d. Any documentation or reports specifically identified in this contract as deliverable work products <br /> shall be retained as in 4.a., above. <br /> e. All field and laboratory records that are associated with work performed under this contract shall <br /> be organized so that any information can be quickly and easily retrieved for inspection, copying or <br /> distribution. <br /> f. The Department reserves the right to request some or all of the laboratory or field information in <br /> an electronic format specified by the Department, as specified in the contract, and/or as <br /> described in the approved contract QA plan(section 6).Also see subsection k., below. <br /> g. Any certified laboratory reports issued for contracted sample analyses using certified methods <br /> shall be generated in accordance with NELAC Quality Systems requirements (NELAC 2003, <br /> section 5.5.10). <br /> h. Upon request by the Department contract manager or as required by the contract, copies of the <br /> original laboratory reports shall be submitted to the contract manager. <br /> i. In addition to any reports of sample results provided per contract deliverable requirements and <br /> subsections b., e., f. and g., above, the contractor shall submit any of the laboratory information <br /> and/or records associated with the contracted analyses as described in this section (section 4) <br /> upon request by DEP, including any of the following: <br /> r Laboratory sample identification(ID)and associated Field ID <br /> ► Analytical/test method <br /> ► Parameter/analyte name <br /> ► Analytical result(including dilution factor) <br /> ► Result unit <br /> ► Applicable DEP Data Qualifier Codes per Table 1 of Chapter 62-160, F.A.C. <br /> ► Result comment(s) to include corrective/preventive actions taken for any failed QC <br /> measure (e.g., QC sample result, calibration failure) or other problem related to the <br /> analysis of the samples <br /> ► Date and time of sample preparation(if applicable) <br /> ► Date and time of sample analysis <br /> ► Results of laboratory verification of field preservation of received samples <br /> ► Sample matrix <br /> ► DoH ELCP certification number for each laboratory (must be associated with the test <br /> results generated by each laboratory analyzing samples under this contract) <br /> ► MDL, Limit of Detection(LOD)or other defined limit of detection <br /> ► PQL, Limit of Quantitation(LOQ)or other defined limit of quantification <br /> ► Field and laboratory QC blank results: <br /> • Laboratory QC blank analysis results as required by the method and the NELAC <br /> Quality Systems standards(e.g., method blank) <br /> • Results for trip blanks, field blanks and equipment blanks, as applicable to the <br /> project and as specified in the QA Plan(see Section 6) <br /> r Results for field duplicates(or replicates) <br /> ► Results for other QC and calibration verification results, as applicable to the specific test <br /> methods used for the contracted analyses: <br /> • Results of sample matrix spikes, laboratory duplicates or matrix spike duplicates <br /> • Results of surrogate spike analyses <br /> • Results of laboratory control samples(LCS) <br /> • Results of calibration verifications <br /> • Acceptance criteria used to evaluate each reported quality control measure <br /> Exhibit E,Page 3 of 6 <br /> DEP Quality Assurance Requirements for Contracts&Grants <br /> Standard Field&Lab Services <br /> Rev. 1-19-16 <br />