Evaluating Laboratory Data. Tom Frick Environmental Assessment Section Bureau of Laboratories



Similar documents
APPENDIX N. Data Validation Using Data Descriptors

ASSURING THE QUALITY OF TEST RESULTS

QUALITY ASSURANCE / QUALITY CONTROL POLICY BREG SOIL AND WATER QUALITY LABORATORY UNIVERSITY OF DELAWARE

1 Quality Assurance and Quality Control Project Plan

Ecology Quality Assurance Glossary

Data Quality. Tips for getting it, keeping it, proving it! Central Coast Ambient Monitoring Program

Medical Cannabis Laboratory Approval Program

APPENDIX 7-B SUGGESTED OUTLINE OF A QUALITY ASSURANCE PROJECT PLAN

American Association for Laboratory Accreditation

STANDARD OPERATING PROCEDURES

DATA QUALITY OBJECTIVES

Pace Analytical e-report

FOOD FOR THOUGHT Topical Insights from our Subject Matter Experts UNDERSTANDING WHAT IS NEEDED TO PRODUCE QUALITY DATA

ANALYTICAL DETECTION LIMIT GUIDANCE. & Laboratory Guide for Determining Method Detection Limits

Validation and Calibration. Definitions and Terminology

CHAPTER ONE TABLE OF CONTENTS 1.0 INTRODUCTION... 1

How to Verify Performance Specifications

Guidelines for Quality Assurance and Quality Control in Surface Water Quality Programs in Alberta

Content Sheet 7-1: Overview of Quality Control for Quantitative Tests

Procedure for Writing Technical Procedures

Building Credibility: Quality Assurance & Quality Control for Volunteer Monitoring Programs

Determination of Total Suspended Solids (TSS) and Total Volatile Solids (TVS) in Waters of Fresh/Estuarine/Coastal Waters

Introduction. The following definitions may help you better understand the components of the data report.

Quality Assurance/Quality Control in Acid Deposition Monitoring

DATA VALIDATION STANDARD OPERATING PROCEDURES FOR CONTRACT LABORATORY PROGRAM ROUTINE ANALYTICAL SERVICES

Laboratory Quality Assurance Manual

Approvals [Signature On File]

P07 CALA Application of Requirements in ISO/IEC 17025:2005 Revision 3.4 April 9, 2014

Proficiency Testing In A Global Analytical Environment Benefits & Challenges. AOAC September 2007

Control Charts and Trend Analysis for ISO Speakers: New York State Food Laboratory s Quality Assurance Team

Step-by-Step Analytical Methods Validation and Protocol in the Quality System Compliance Industry

Developing Quality Assurance Project Plans using Data Quality Objectives and other planning tools. Developing QAPPs 5/10/2012 1

PERFORMANCE EVALUATION AUDIT CHECKLIST EXAMPLE. EIIP Volume VI

Quality Assurance (QA) & Quality Control (QC)

Technical Guidance Manual for the Implementation of the Hawai`i State Contingency Plan. Interim Final SECTION 10

9. Quality Assurance 9.1 INTRODUCTION 9.2 FIELD SAMPLING QUALITY ASSURANCE 9.3 ANALYTICAL QUALITY ASSURANCE Internal Quality Control

QUALITY ASSURANCE PROJECT PLAN FOR BROWNFIELDS/VOLUNTARY CLEANUP PROGRAM SITES

Method Validation/Verification. CAP/CLIA regulated methods at Texas Department of State Health Services Laboratory

Quality Assurance Manual

Rounding and Significant Figures

DATA QUALITY ASSESSMENT AND DATA USABILITY EVALUATION TECHNICAL GUIDANCE

APPENDIX L DATA VALIDATION REPORT

Radioanalytical Data Validation Issues and Solutions

METHOD 9075 TEST METHOD FOR TOTAL CHLORINE IN NEW AND USED PETROLEUM PRODUCTS BY X-RAY FLUORESCENCE SPECTROMETRY (XRF)

1. PURPOSE To provide a written procedure for laboratory proficiency testing requirements and reporting.

Quality Assurance Plan

DRY CLEANING PROGRAM QUALITY ASSURANCE MANAGEMENT PLAN

Third Party Data Validation: What you need to know and do!

Samples RMN Analytical Report ( ) GC/FID Analysis (RM01) Nicotine Purity

UNITED STATES CONSUMER PRODUCT SAFETY COMMISSION DIRECTORATE FOR LABORATORY SCIENCES DIVISION OF CHEMISTRY 5 RESEARCH PLACE ROCKVILLE, MD 20850

EPA GUIDANCE FOR QUALITY ASSURANCE PROJECT PLANS EPA QA/G-5

APPLICATION OF ICP-MS TECHNOLOGY FOR TRACE METALS ANALYSIS

Analytical Data Package Reports

Signal, Noise, and Detection Limits in Mass Spectrometry

Data Quality Objectives and Quality Assurance Project

Commonwealth of Kentucky. Wastewater Laboratory Certification Manual

Assay Qualification Template for Host Cell Protein ELISA

Gap Analysis of ISO 15189:2012 and ISO 15189:2007 in the field of Medical Testing

Innovative Technology Verification Report

Canadian Environmental Technology Verification Program Applicant Information Package CONTENTS

EPA NATIONAL LEAD LABORATORY ACCREDITATION PROGRAM. LABORATORY QUALITY SYSTEM REQUIREMENTS (LQSR) REVISION 3.0 (November 05, 2007)

Minnesota Pollution Control Agency. Quality Assurance Project Plan Guidance

APPENDIX C. DATA VALIDATION REPORT

Appendix B. Eugene/Springfield Environmental Services Laboratory Quality Assurance Plan

2010 Laboratory Accreditation Program Audioconference. Accreditation Requirements for Waived Vs. Non-waived Tests

Glossary. Acceptable Value - An observed or corrected value that falls within the acceptable range.

PERFORMANCE-BASED EVALUATION OF LABORATORY QUALITY SYSTEMS An Objective Tool to Identify QA Program Elements that Actually Impact Data Quality

Standard Operating Procedure for Database Operations

M E M O R A N D U M. Austin Police Department Field Support Services Forensic Science Division

Appendix C Data Validation Report

Electronic Data Validation Using the Locus Environmental Information Management System. Tricia Walters Locus Technologies

Drip Club 2540 Corporate Place, Suite B103 Monterey Park, CA 91754

RTP s NUCLEAR QUALITY ASSURANCE PROGRAM

MIDLAND AREA SOIL SAMPLING MIDLAND, MICHIGAN

Quality Assurance Plan

Bryte Chemical Laboratory Quality Assurance Manual

CERTIFICATE OF ANALYSIS

QUALITY ASSURANCE PLAN

Data Management Implementation Plan

Sample Analysis Design Step 2 Calibration/Standard Preparation Choice of calibration method dependent upon several factors:

State Meat and Poultry Inspection (MPI) Program Laboratory Quality Management System Checklist

Drinking Water Analytical Method and Program Requirements: Roles and Responsibilities, Analytical Method Approval, and Effective Oversight

COPY. Revision History: Changes were made to reflect the current practice of only including the most recent changes in the revision history.

USE OF REFERENCE MATERIALS IN THE LABORATORY

LAB ID and/or LABORATORY NAME: ASSESSOR NAME: CONTINUOUS RADON MONITOR (CRM) by Proportional Counting. Method Number: ELAP method code 7037

Laboratory Procedure Manual

Analytical Procedures and Method Validation

Laboratory Director Responsibilities

Quality Assurance For Environmental Laboratories

Working Copy - 1,- / t&,1 r. Responsibilities of the Laboratory Quality Assurance Officer. EffectiveDate: 7/ltl/ l'rritials: tuwt

NC SBI QUALITY ASSURANCE PROGRAM

TEST REPORT: SIEVERS M-SERIES PERFORMANCE SPECIFICATIONS

Transcription:

Evaluating Laboratory Data Tom Frick Environmental Assessment Section Bureau of Laboratories

Overview of Presentation Lab operations review QA requirements MDLs/ PQLs

Why do we sample? Protect physical, chemical, and biological integrity (Clean Water Act) Water quality standards, 62-302 FAC Permit compliance Interpret biological community results

How Do You Measure an Collect sample Prepare sample Analyte? Calibrate equipment Measure analyte Compare analyte measurement to known standard Run Quality Control samples

Proper location Correct equipment or bottles Prevent contamination Proper preservation

Sample log-in & tracking (1000 s per day) Preparation steps Holding times Pairing sample with result and QC elements

Calibration & maintenance Blank contamination Spike recovery Detection limits Statistically, QC failures occur routinely

Bottom Line on Lab Measurements Literally 1000 s of different methods to measure various types of analytes. Each method has specific quality control requirements to assure valid measurements.

Required Laboratory Quality Control Activities

QA Requirements for Laboratories, Rule 62-160 NELAC Certification Performance Test Samples Mandatory Quality Control Ethics and training Reporting Location, methods, QA elements (extensive list) Audits Lab, field, document review, corrective action Data validation Completeness, data integrity & usability

Performance Test Samples NELAC required Blind sample, lab does not know concentration of analyte. Lab runs PT sample using routine procedures. Must achieve acceptable result in 2 of 3 previous PTs. Unknown Result must be within range

Instrument Response Calibration Establishing a relationship between instrument response and known concentrations. Regression line R 2 should be 0.995 or better Concentration

Continuing Calibration Verification Instrument Response Calibration must be rechecked every 20 samples. Real value = 1.0 ug/l Usually required to be + or 5 to 15%. Concentration 0.99 ug/l

Lab Blank Analyte-free water processed as routine sample. Result evaluated to determine sources of internal lab contamination. Analyte-free water Result evaluated, should be U

Accuracy and Precision Accuracy: The ability to measure the true value. True value is NIST standard Precision: Consistency of Measurements.

Lab Control Sample (LCS) A known concentration of analyte added Sample processed routinely. Determine if amount detected matches amount added (+ or acceptable %). Add known Amount (spike) Determine % recovery Acceptance criteria is usually 80% to 120%

Lab Control Sample Duplicate Add known amount Split Compare results, determine precision

Why Quality Control Samples are Important Good precision, Good accuracy Good precision, Poor accuracy Poor precision, Good accuracy Poor precision, Poor accuracy

Accuracy The true or standard value is based on the central tendency of measurements involving multiple high quality testing laboratories, using exacting NIST procedures. Other laboratories purchase standards for calibration and QC. 1.0 ug/l

Precision The relative agreement in values from repeated measures of the same sample (relative standard deviation) during routine testing runs (measurement repeatability). Tight, acceptable precision Noisy, unacceptable precision

To Ensure the Correct Decision: DEP must verify that data are useable. Consistent with Data Quality Objectives and program requirements. We have Statutory Authority to reject data!!!

Data Quality & DEP If real result is higher than reported Environment is not protected If real result is lower than reported Costly, unneeded treatment requirements In either case: Legal challenges Adverse publicity Ultimately Results in More Staff Time and $$

Detection and Quantitation Limit Concepts

Definitions Minimum Detection Limit: The minimum concentration that can be measured with 99% confidence that the analyte concentration is greater than zero. Practical Quantitation Limit: The lowest level of measurement that can be reliably achieved during routine laboratory operating conditions within specified limits of precision and accuracy.

Radio Tower MDL/PQL Radio Reception Analogy Whole sentences, complete comprehension > PQL A few words, but no meaning = MDL Static Only: < MDL I, M U,T

Simplified MDL Study Take analyte free water or low level spikes and place in 7 containers Process as normal samples All prep steps, reagents, instrument calibration, etc. are routine Generate results Calculate standard deviation of results MDL is 3 times this SD This is the 99% confidence limit that you can distinguish signal from noise

Theoretical Probability Distributions Analytical Noise 0.4 Noise Distribution MDL set to exclude 99% of the Noise Distribution 0.3 Frequency 0.2 MDL 0.1 0.0-2 0 2 4 6 8 Standard Deviations

MDL for More Sensitive Method MDL for Less Sensitive Method

Method 1631 MDL by 40 CFR Method 0.04 0.03 0.02 Mercury ( n g /L ) 0.01 0-0.01-0.02-0.03-0.04 January - March

MDL/PQL Relationship Concentration Present Absent 0 M I U T Region of known precision and accuracy PQL (4 x MDL) = 4 x 0.3 = 1.2 ug/l Region of high uncertainty for quantitation (greater certainty as PQL is approached) MDL (3 x SD) = 3 x.1 = 0.3 ug/l Use MDL as an Estimate of a Lab s Ability to Detect (not quantitate) at the MDL concentration

POSSIBLE DECISIONS Detected TRUE SITUATION Analyte Present CORRECT DECISION Analyte Not Present INCORRECT DECISION FALSE POSITIVE (Type I error) Not Detected INCORRECT DECISION FALSE NEGATIVE (Type II error) CORRECT DECISION

Detection Limit Values U Values > Permit Limits? Method may not be appropriate; Use more sensitive method (if available) Matrix interference or dilution may contribute to an elevated detection limit I or M Values Near Permit Limits Compliance Issue? May Require Additional Testing to Resolve

62-4.246 FAC PQL, MDL and Compliance Refers to checklist of DEP approved MDLs Results > PQL are reported as measured Results < PQL and > MDL shall be deemed as = to the MDL Results < MDL shall be reported as non-detects ( U )

Co Co ncentrati ncentrati on on Interpreting 62-4.246 FAC: Examples Result Permit Limit PQL Permit Limit Result PQL MDL MDL Non- Compliance Compliance

Concentr Concentr ation ation Interpreting 62-4.246 FAC: Examples PQL Result Permit Limit MDL Compliance (Results < PQL are deemed = MDL) PQL Permit Limit Result MDL Compliance

Concentr Concentr ation ation Interpreting 62-4.246 FAC: Examples PQL Result MDL Permit Limit PQL Result is Non-detect MDL Permit Limit Non-Compliance Compliance

Tom Frick (850) 245-8065 thomas.frick@dep.state.fl.us Quality of Science enewsletter http://www.dep.state.fl.us/labs/training/listserve.htm