Current through Register Vol. 56, No. 24, December 18, 2024
Section 7:26E-2.2 - Quality assurance project plan(a) The person responsible for conducting the remediation shall prepare and follow a quality assurance project plan for all sample and data collection.(b) The person responsible for conducting the remediation shall include the following in a quality assurance project plan: 2. Site specific project and data quality objectives;3. A sample design and rationale, including where samples will be taken;4. The names and contact information of the following project specific personnel:ii. The quality assurance coordinator;iii. The health and safety coordinator;iv. Identification of laboratory(ies) that will be used for sample analyses including certification number(s); and5. A sample summary table containing (at a minimum) the following: ii. Analytical parameters;iii. The number of samples for each matrix;iv. The frequency of sample collection;v. The number and frequency of field/trip blanks; andvi. The number and frequency of duplicate samples;6. A detailed description of sampling methodologies for each matrix tested along with standard operating procedures references;7. Field documentation procedures;8. A list of all field instrumentation being utilized;9. Inclusion of a reference to a standard operating procedure that describes the operation of all field instrumentation being utilized including: i. Calibration procedures;ii. Calibration check procedures;v. Preventative maintenance; andvi. A detailed description of field quality assurance/quality control procedures;10. A detailed description of sample handling and chain-of-custody procedures;11. A detailed description of field storage and transport procedures;12. A sample container/preservation/holding time table including: i. Sample volumes to be collected per matrix;ii. Sample containers used per matrix;iii. Sample preservation required per method and matrix; andiv. Sample holding times;13. An analytical methods summary table listing all analytical methods to be used to analyze all samples;14. Project compounds summary including: i. A list of compounds by method and matrix;ii. Project action limits by method and matrix; andiii. Project quantitation limits denoting analytical sensitivity requirements by method and matrix;15. Measurement performance criteria and quality control samples to be used by method and matrix;16. Quality assurance and quality control requirements for analysis;17. Laboratory data deliverable formats to be used;18. The procedure for review (verification and usability procedures), including data assessment versus stated data quality objectives of laboratory data;19. A discussion of how corrective action procedures are to be implemented and documented relative to potential deviations to the project quality objectives;20. A detailed description of the laboratories quality assurance/quality control procedures; and21. Data and records management and archive procedures.N.J. Admin. Code § 7:26E-2.2