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ANNEX IU.K.THE OECD PRINCIPLES OF GOOD LABORATORY PRACTICE (GLP)
SECTION IIU.K.GOOD LABORATORY PRACTICE PRINCIPLES
3.FacilitiesU.K.
3.1.GeneralU.K.
1.The test facility should be of suitable size, construction and location to meet the requirements of the study and to minimise disturbance that would interfere with the validity of the study.U.K.
2.The design of the test facility should provide an adequate degree of separation of the different activities to assure the proper conduct of each study.U.K.
3.2.Test system facilitiesU.K.
1.The test facility should have a sufficient number of rooms or areas to assure the isolation of test systems and the isolation of individual projects, involving substances or organisms known to be or suspected of being biohazardous.U.K.
2.Suitable rooms or areas should be available for the diagnosis, treatment and control of diseases, in order to ensure that there is no unacceptable degree of deterioration of test systems.U.K.
3.There should be storage rooms or areas as needed for supplies and equipment. Storage rooms or areas should be separated from rooms or areas housing the test systems and should provide adequate protection against infestation, contamination, and/or deterioration.U.K.
3.3.Facilities for handling test and reference itemsU.K.
1.To prevent contamination or mix-ups, there should be separate rooms or areas for receipt and storage of the test and reference items, and mixing of the test items with a vehicle.U.K.
2.Storage rooms or areas for the test items should be separate from rooms or areas containing the test systems. They should be adequate to preserve identity, concentration, purity, and stability, and ensure safe storage for hazardous substances.U.K.
3.4.Archive facilitiesU.K.
Archive facilities should be provided for the secure storage and retrieval of study plans, raw data, final reports, samples of test items and specimens. Archive design and archive conditions should protect contents from untimely deterioration.
3.5.Waste disposalU.K.
Handling and disposal of wastes should be carried out in such a way as not to jeopardise the integrity of studies. This includes provision for appropriate collection, storage and disposal facilities, and decontamination and transportation procedures.