NYC 9/11 Public Portal Document
Part II - Environmental Community Monitoring Plan
133-135 Greenwich & 21-23 Thames Streets
Airtek Project 05-0701— Rev 2 September 16, 2005
Performs validation checks for timeliness, completeness and correctness for all hard copy
data reports.
Reviews Quality Assurance Quality Control (QA/QC) measures such as percent recoveries,
duplicate analyses and laboratory blanks reported in the hard copy data reports.
2.6 Records
2.&1 Records Created
The following records may be created by this procedure:
• Field Activity Logs
• Sample and Composite Collection forms and/or field logs
• Chain-of-Custody Forms
• Shipping documents
• Laboratory analysis results
• Electronic files.
2.6,2 Records Retention
The Airtek Quality Coordinator retains hard copies of all the records created by this
procedure.
The Data Manager maintains electronic records and ensures that periodic backups and
archiving of electronic files is done.
2.6.3 Records Care and Maintenance
The Airtek Quality Coordinator is responsible for the care, maintenance, and disposition of
records according to Airtek record management policies and procedures.
Records must be retained in an organized system so that the records are protected and easily
accessed when needed.
2.6,4 When Records Transferred to Archivesfor Storage
All records created by this procedure are reviewed after three years for transfer to the Airtek
Archives.
3.0 QUALITY ASSURANCE PROCEDURES
All samples will be immediately placed in storage/transport containers or housings following
completion of the sampling period and prior to being recorded on chain-of-custody forms and
placed in chilled coolers. Samples will be preserved according to the specific method
requirements and delivered to the laboratory within 24 hours of collection.
Daily field audits will be carried out by a designated QA Coordinator to ensure compliance
during the performance of the sampling procedures. QA Coordinator will note and will bring to
the attention of the Field Manager and the Project Manager any deviations from the approved
plans. All deviations will be recorded in the QA Coordinator's log and in the field notebook of
the sampling team being audited.
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