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    Management en Good Laboratory Practice op de afdeling Biotechnische Evaluatie Stofeffecten (BES) van het Centraal Dierenlaboratorium (CDL)

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    Authors
    van Soolingen J
    Kroes 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
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    Type
    Report
    Language
    nl
    
    Metadata
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    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
    Publiekssamenvatting
    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>
    Publisher
    Rijksinstituut voor Volksgezondheid en Milieu RIVM
    Sponsors
    RIVM
    URI
    http://hdl.handle.net/10029/260036
    Collections
    RIVM official reports

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