Management en Good Laboratory Practice op de afdeling Biotechnische Evaluatie Stofeffecten (BES) van het Centraal Dierenlaboratorium (CDL)
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Series / Report no.
Open Access
Type
Report
Language
nl
Date
1992-05-31
Research Projects
Organizational Units
Journal Issue
Title
Management en Good Laboratory Practice op de afdeling Biotechnische Evaluatie Stofeffecten (BES) van het Centraal Dierenlaboratorium (CDL)
Translated Title
Management and Good Laboratory Practice at the Division Biological Evaluation of Drug effects of the Central Animal Laboratory
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Abstract
The department BES (Biological Evaluation of Drug Effects) carries out animal studies for RIVM laboratories, whose commitment to GLP makes it necessary for BES also to comply with GLP. Compliance is assured by means of a quality system laid down in a quality handbook quaranteeing the consistent quality of the department products. The elements of the BES quality system are documented in this report under the following headings: - quality targets and management organisation - survey of areas of competence and of stoff qualifications - equipment inventory - goods and services available - standard operating procedures. Furthermore a general servey is presented of those co-operative arrangements necessary for optimal departmental organization.<br>
Description
Publisher
Rijksinstituut voor Volksgezondheid en Milieu RIVM
Sponsors
RIVM