TY  - BOOK
AU  - Weinberg,Sandy
TI  - Good laboratory practice regulations
SN  - 0824708911 (alk. paper)
AV  - R850 .G66 2003
U1  - 615.19 
PY  - 2003///
CY  - New York
PB  - Marcel Dekker
KW  - Medical laboratories
KW  - Quality control
KW  - Pharmaceutical technology
N1  - Includes bibliographical references (p. 229-237) and index; TOC; Historical Perspective, Jean M. Taylor and Gary C. SteinFDA/ GLP Regulations, Wendell A. PetersonApplying 21 CFR Part 11 to the Laboratory Environment, Sandy WeinbergThe Good Automated Laboratory Practices, Gerald J. Whartenby, Paul L. Robinson, and Sandy WeinbergImplementing GLP's in a Non-GLP Analytical Laboratory, Stephanie A. OlexaComputer Systems Validation, Sandy WeinbergThe FDA's GLP Inspection Program, George W. JamesThe Future, Sandy WeinbergBibliographyIndex; Pharmacy
N2  - Summary:
Covers all aspects of the Food and Drug Administration's (FDA), Good Laboratory Practice (GLP) regulations and techniques for implementation. This book details standards and general guidelines for the management of research environment. It examines theoretical principles for anticipating interpretations of GLP in a variety of laboratory settings
UR  - http://www.loc.gov/catdir/enhancements/fy0647/2002035159-d.html
UR  - http://lib.ewubd.edu/ebook/4689
ER  -