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Good Laboratory Practice
Test facilities included in the Netherlands' GLP monitoring program
Annual overviews of the test facilities inspected, their GLP status and areas of expertise will be prepared each year and sent to the national regulatory authorities and foreign GLP monitoring authorities. The latest reports are available here:
Domestic test facilities included in the GLP monitoring program
Foreign non-domestic test facilities included in the GLP monitoring program
Legends to the abbreviations used:
TEST FACILITY
Full name and address of the test facility
DATE OF INSPECTION
Month and year of the inspection / study audit
STATUS
GLP compliance status of the test facility:
- IC -In Compliance: no or only minor deviations from the GLP principles have been observed, which have been corrected during the inspection or within 1 month following the inspection.
- PEN -Pending: Deviations from the GLP principles have been observed which could not be corrected within a month after the inspection. No major impact expected on the reliability of data produced by the test facility; correction of the deviations possible within 1-6 months; sometimes re-inspection necessary (to be specified).
- NIC -Not in compliance: Major deviations from the GLP principles have been observed. Procedures in the test facility are such that the reliability of data cannot be ensured.
- RFP -Removed from program: test facility is removed from GLP monitoring program
NATURE OF INSPECTION
FAC -Facility inspection
SA -Study Audit
FULL -Full inspection of facilities and studies (FAC+SA)
RE-I -Re-inspection as follow-up to a full inspection
AREA OF EXPERTISE
1 - Physical-Chemical testing
2 -Toxicity studies
3 - Mutagenicity studies
4 - Environmental toxicity studies on aquatic and terrestrial organisms
5 - Studies on behaviour in water, soil and air; bio-accumulation
6 - Residue studies
7 - Studies on effects on mesocosms and natural ecosystems
8 - Analytical and clinical chemistry
9 - Other studies, specified
REMARKS
Complementary information
