N.J. Admin. Code § 7:18-8.5 - Requirements for records and data reporting
(a) The
laboratory shall retain records concerning analyze-immediately and continuous
monitoring analyses. The records to be retained include raw data records,
quality control data records, chain-of-custody forms, laboratory reports, and
the information required under (d) below. The laboratory shall retain each
record for at least five years after the date of the analysis, provided,
however, that the laboratory shall retain records of analyses for 10 years if
the person requesting the analyses has informed the laboratory that the
analyses were to be performed because of epidemiological or public health
concerns.
(b) The laboratory shall
file and maintain data and other records in an accessible location on the
laboratory's premises for one year after the date of analysis so that reviews
can be conducted during on-site audits.
(c) The laboratory shall retain the following
information as part of the records of analysis:
1. The assigned laboratory sample number or
other unique form of identification;
2. The date and time of sample
analysis;
3. The name and signature
of the person or persons who collected the sample;
4. The name and signature of the person or
persons who analyzed the sample;
5.
The type of analysis performed and the DSAM used; and
6. The results of the analysis and the raw
data generated by the analysis.
(d) The laboratory shall check all results
reported on final report forms against original data to make sure there are no
transcription errors.
(e) The
laboratory shall include the following information in reporting results to the
client:
1. The certified environmental
laboratory name and New Jersey laboratory identification number;
2. The date, time, and location of sample
collection and sample analysis;
3.
The type of analysis performed and the analytical method employed;
4. The results generated by the analysis;
and
5. The name and signature of
the environmental laboratory manager or designee identified under
7:18-2.11(a)1
iii.
(f) The laboratory
shall not report results of analyses to the Department or to any other person
unless the original or true duplicate of the results is sent to the client. The
report shall be signed by the laboratory manager or designee identified under
7:18-2.11(a)1
iii.
Notes
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