Title: Laboratory Ethics
1Laboratory Ethics Data Integrity
- Presentation to KWWOA
- April 2, 2008
- Department for Environmental ProtectionEnvironmen
tal Public Protection Cabinet
To Protect and Enhance Kentuckys Environment
2Science Fraud
- Of all the violations of the ethos of science,
fraud is the gravest. As with error, fraud
breaks the vital link between human understanding
and the empirical world, a link that is sciences
greatest strength. But fraud goes beyond error
to erode the foundation of trust on which science
is built. (Committee on the Conduct of Science,
1989)
3Laboratory Ethics and Data Integrity
4Laboratory Fraud
- Defined as
- the deliberate falsification of analytical and
quality assurance results, where failed method
and contractual requirements are made to appear
acceptable during reporting.
5Ethical Behavior
- Defined as
- Behavior that conforms to accepted professional
standards of conduct unethical behavior
therefore is behavior not conforming to those
standards.
6Bad and Fraudulent Data
- Incorrect data may either be the result of bad
techniques, training or human error. - Fraudulent data is the result of an individual
purposefully misrepresenting data that does not
conform to a given set of standards or criteria
and making it appear as if it does.
7Unethical Conduct Being Addressed
- ACS
- NELAC / AOAC
- ISO / IEC 17025
- EPA
- DoD
- Primacy States
- Private Industry
8Producers of Laboratory Data
- Field / Sample Technicians
- Sample Custodian
- Laboratory Chemists / Technicians
- Report Generation Group
- LIMS / Information Technology
- Laboratory Managers
9Data Users
- Plant Operators
- Plant Supervisors / Managers
- Regulators
- General Public
10Data Checks and Balances
- Laboratory Chemists / Technicians
- Laboratory Quality Assurance Dept.
- Laboratory Managers
- Data Validator (Third Party)
- Auditor (In-house / Third Party)
- Regulators
11Life Cycle of a Water Sample
- Sample Collection
- Sample Analysis
- Sample Report
- Operator
- Operation / Plant Decisions
- Results Reported to State Regulator
- Public Information
- State Reports Results to EPA
- Records Retention
12Legacy of Sample Results
- Laboratory Files (hardcopy)
- Laboratory Notebooks
- Magnetic Tape (Electronic media)
- Plant Files
- State Files Database
- EPA Database
13Fraudulent Data Takes Many Forms
- Dry Labbing
- Time Traveling
- Juicing
- Improper GC/MS Tuning
- Improper Calibration / QC Analysis
- Peak Shaving
- Misrepresentation of QC Samples and Spikes
- File substitution
- Unwarranted Manipulation of Computer Software
- Improper Alteration of Analytical Conditions
- Over Dilution of Samples or Misrepresentation of
Detection Limits - Deletion of Non-Compliant Data
- Concealment of a Known Problem
14Why?
- Shrinking Market
- Low Prices Cutting Corners
- Insufficient Resources / Training
- Unclear Management Position
- Employee Perception
- Employee Personal Issues
15Repercussions
- Inaccurate or inappropriate changes to plant
operating conditions - Incorrect data reported to regulators
- May place public at risk
- Criminal implications
- Employment consequences
16Laboratory Ethics and Data Integrity
17Certified Laboratories
- Adopt Best Practices for the Detection and
Deterrence of Laboratory Fraud - Establish Ethics and Data Integrity Policy
- Utilize Contractual Agreements
- Adopt QAPP, SAMP, DQO and SOP
- Consider Third-Party Experts
18Ethics Data Integrity Policy
- Laboratories should have a company ethics policy
read and signed by all employees - Training should be provided to staff
- Specific SOPs for each method performed by the
laboratory should be written and maintained - Laboratory management must provide adequate
resources and assign sufficient authority to
supervisors
19What Labs Can Do - Ethics
- Ethics Compliance Plan
- Ethics Policy or Statement
- Employee Ethics Agreements
- Ethics Training Communication
- Ethics Program Management
- Ethics Procedures (assistance and reporting
mechanism) - Zero Tolerance Policy
- Compliance Audits
20What Labs Can Do Non Tangible
- Ensure Capacity
- Ensure Responsibility and Authority
- Demonstrate Accountability
- Scientific Approach
- Maintain Objectivity
- Maintain Impartiality
- Measurement Traceability
- Reproducibility
- Transparency
21EPA Guidance and Training
- Developing an SOP for detecting and reporting
potentially fraudulent laboratory activities - Fraud awareness workshops
- Increasing scrutiny by data reviewers /
validators - EPA Fraud Hotline 1-888-546-8740
- Developing a fraud profile checklist for on-site
auditors to prompt auditors to look for
indicators of potential fraud - Requiring use of bound laboratory notebooks
- http//www.epa.gov/QUALITY/qa_docs.html
22QAPP, SAMP, DQO and SOP
- Prepare Project Specific Documents Tailored To
Sampling / Analytical Requirements - Update Documents at Least Annually
- Make Documents Available to Necessary Personnel
(Field, Lab, etc) - Reference Documents in Contract Agreements
23Quality Assurance Project Plan
- EPA Requirements for Quality Assurance Project
Plans (QAPPs) EPA QA/R-5 March 2001
EPA/240/B-01/003 - EPA Guidance for Quality Assurance Project Plans
(QAPPs) EPA QA/G-5 December 2002
EPA/240/R-02/009
24Sampling, Analysis Monitoring Plan
- Guidance on Choosing a Sampling Design for
Environmental Data Collection (QA/G-5S) December
2002 EPA/240/R-02/005.
25Data Quality Objectives
- EPA Guidance on Systematic Planning using the
Data Quality Objectives Process (QA/G-4)
February 2006EPA/240/B-06/001 - Provide a fundamental role in data collection
activities - Allows decision makers to define their data
requirements and acceptable levels of data error,
based on intended use of data - Specifies relevant data quality requirements
which could potentially impact data use
limitations - DQO process minimizes expenditures while
producing data of sufficient quality for its
intended use
26Standard Operating Procedures
- EPA Guidance for Preparing Standard Operating
Procedures (SOPs) EPA QA/G-6 April 2007
EPA/600/B-07/001
27What PWS Can Do
- Utilize more than one laboratory
- Contractual agreements
- Consider third-party experts
28Use More Than One Laboratory
- Reduces / eliminates overload
- Split-sample opportunities
- Similar results build confidence with clients
- Helps ensure that key decisions are not based on
a single data source
29Contractual Agreements
- Boiler plate language is available
- QA/QC requirements
- DQO requirements
- Specify intended use of data
- Pertinent documents must be included (or
referenced) in the agreement
30Consider Third-Party Experts
- Perform on-site evaluations (audits)
- Provide added value to program
- Additional cost
- Independent parties with respect to business
decisions, laboratory, findings, final report,
etc. - Deterrent to potential fraud
31Report Fraud in Kentucky
- EPPC Office of the Inspector General
- OIG Hotline 1-888-564-0498
32Questions
33Contact Information
- Patrick J. Garrity
- Certification Officer Division of Water14
Reilly Road - Frankfort, KY 40601
- Phone (502) 564-3410 ext. 574
- Fax (502) 564-2741
- Email patrick.garrity_at_ky.gov