Management en Good Laboratory Practice op de afdeling Biotechnische Evaluatie Stofeffecten (BES) van het Centraal Dierenlaboratorium (CDL)
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Authors
van Soolingen JKroes R
de Vrey P
Arens ABM
Beenen J
Bekius FA
Gomersbach-de Ridder A
Jansen van 't Land C
van de Kuil R
ter Laak BG
de Liefde A
Luypen SW
Mattern PF
Poelen MJ
Post W
Reulen P
van de Siepkamp JJ
Schot CW
Timmerman A
van Veenendaal W
Type
ReportLanguage
nl
Metadata
Show full item recordTitle
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 LaboratoryPubliekssamenvatting
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>Sponsors
RIVMCollections