62-160.600. Research Field and Laboratory Procedures  


Effective on Monday, April 16, 2018
  • 1(1) Research field sampling and laboratory procedures involve one or more of the following:

    15(a) Evaluation, development or use of new, innovative technologies not yet approved by the Department;

    30(b) Evaluation, development or use of innovative field sampling or analytical laboratory methods not yet approved by the Department;

    49(c) Evaluation of new methodology or technology to be used in lieu of a Department-approved method 65described in subsection 6862-160.320(1), 69F.A.C.; 70and,

    71(d) Other projects not included in the above areas but designated as research by the relevant Department project or contract manager.

    92(2) If a research field sampling or laboratory method is being developed for subsequent use in compliance or other regulatory activities, the method shall be reviewed and approved according to the requirements provided in Rules 12762-160.220 128and 12962-160.330, 130F.A.C.

    131(3) All research field sampling and laboratory procedures shall be described in a Department-approved work or study plan or in direct contract language. The following minimum elements shall be addressed, as applicable:

    163(a) Project purpose and intended end use of the data, 173such as 175specific hypotheses 177and topics to be investigated;

    182(b) Brief historical overview or literature searches;

    189(c) Statement of anticipated results or effects of the research project;

    200(d) Description of work to be conducted, including the types of analyses to be performed to monitor the effectiveness of the research;

    222(e) The information and records to be included in the data report package and the reporting format for hard copy and electronic reports, 245such as all documentation to be delivered to the Department as work product as required by a grant or contract265. Minimum requirements for record keeping shall follow those specified in Rules 27762-160.240 278and 27962-160.340, 280F.A.C., as applicable;

    283(f) Identification of any specialized training or certification needed by personnel in order to successfully complete the project or task. This requirement includes specifying any laboratory certification requirements as provided in Rule 31562-160.300, 316F.A.C. However, the Department project manager may waive the requirement for laboratory certification as provided in paragraph 33362-160.300(5)(e), 334F.A.C.

    335(g) All aspects of data generation and acquisition to ensure appropriate methods for sampling, 349sample preservation, sample storage conditions and maximum holding (storage) time limits, 360measurement and analysis, data collection or generation, data handling 369and data storage procedures, 373and quality assurance and quality control activities are employed and documented;

    384(h) The experimental data generation or data collection design for the project, 396such as398:

    3991. Types and numbers of samples required;

    4062. Design of the sampling network;

    4123. S414ample matrices, s417ampling locations, and 420s421ampling frequencies 423or schedules;

    4254. 426Field or laboratory sample testing or analyses frequencies or schedules;

    4365. 437Topics to be investigated by the research, such as a447nalytes, 448organisms, and populations 451of interest;

    4536. Rationale for the 457experimental or research project 461design;

    4627. Procedures for collecting samples, 467such as 469sample handling, preservation and custody in the field and laboratory, sample transport, sampling equipment specifications, and equipment decontamination procedures;

    4888. Sample preparation (if applicable) and 494field or laboratory testing and 499analytical methods used;

    5029. Quality control activities needed for sampling and analysis, 511such as all quality control measurements, control (acceptance) criteria, 520and 521procedures for 523the assessment of the quality control results; 530and, quality 532control activities for the field and the laboratory, 540such as 542the use of blanks, duplicates, 547replicates, 548matrix spikes, laboratory control samples and surrogates;

    55510. Quality assurance activities that occur after the data collection or generation phase of the project, such as data verification validation, and field and laboratory audits;

    58111. Criteria to be used to objectively and consistently review, verify and validate project data, including the chain of custody for data throughout the life of the project or task;

    61112. Proposed methods to analyze the data 618to evaluate the experimental or research design 625and determine possible anomalies or departures from assumptions established in the planning phase of data collection 641that may affect attainment of the research objectives;

    64913. Statistical and/or other procedures and criteria that will be used to evaluate the experimental data produced by the research to test hypotheses and evaluate endpoints, conclusions or other topics for the research project objectives; and,

    68514. Any additional elements specifically required by the Department project manager.

    696(4) The Department shall conduct a technical review of the project work plan prior to the project’s initiation in order to assess its technical and scientific merit and appropriateness.

    725Rulemaking Authority 727403.061, 728403.0623 FS. 730Law Implemented 732373.026, 733373.309, 734373.409, 735373.413, 736373.414, 737373.416, 738373.4592, 739376.303, 740376.305, 741376.3071, 742403.0623, 743403.0625, 744403.087, 745403.088, 746403.0881, 747403.504, 748403.704, 749403.707, 750403.722, 751403.853 FS. 753History–New 1-1-91, Amended 2-4-93, Formerly 17-160.600, Amended 3-24-96, 10-15-96, 4-9-02, 7-30-14, 4-16-18.

     

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