Record Display for the EPA National Library Catalog

RECORD NUMBER: 22 OF 33

OLS Field Name OLS Field Data
Main Title Quality control and quality assurance procedures for level 1 health effects bioassays /
Other Authors
Author Title of a Work
Brusick, David,
Young, R. R.,
Myhr, B.C.,
Jagannath, D. R.,
Publisher United States Environmental Protection Agency, Industrial Environmental Research Laboratory, United States Environmental Protection Agency, Center for Environmental Research Information
Year Published 1983
Report Number EPA/600-S8-83-034
OCLC Number 899245615
Subjects Biological assay--Quality control.
Internet Access
Description Access URL
http://nepis.epa.gov/Exe/ZyPDF.cgi?Dockey=2000TIZD.PDF
Holdings
Library Call Number Additional Info Location Last
Modified
Checkout
Status
EJBD ARCHIVE EPA 600-S8-83-034 In Binder Headquarters Library/Washington,DC 04/05/2018
EJBD  EPA 600-S8-83-034 Headquarters Library/Washington,DC 05/29/2018
Collation 2 pages ; 28 cm.
Notes
"EPA.600-S8-83-034." "December 1983." Caption title. At head of title: Project Summary.
Contents Notes
The purpose of this project was to develop a quality control (QC) and quality assurance (QA) document for the EPA Level 1 environmental assessment biological testing program. This manual, developed as part of this program, supplements the Level 1 biological testing procedures manual (1). Although the Level 1 procedures manual presents detailed information on sample preparation, bioassay procedures, data evaluation, and sample ranking, the Level 1 manual describes the role and recommended use of laboratory QC and QA procedures in the Level 1 biological testing program. IERL-RTP's QA audit sample program is presented in the QC/QA manual. In this program, audit samples are made available to laboratories wishing to verify proficiency in conducting Level 1 bioassays. Also described is the documentation required for test material sampling, processing, storage, and disposal. The manual identifies protocol steps for each Level 1 health effects bioassay and describes the QC and documentation procedures required to meet the U.S. Food and Drug Administration's Good Laboratory Practice Regulations. In addition to recommendations for QC and QA procedures, the document supplies sample forms which may be used by laboratories that have not developed their own standard data recording forms. QC and QA procedures vary somewhat between laboratories, and this document serves as a model, but should not be viewed as the only acceptable approach to QC and QA. These QC and QA procedures are not intended to restrict test performance or improvements in study designs, but are critical to maintain uniformity of data generation, documentation, and interpretation.