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Zdrowie i gospodarka · 21/12/2010

Good Laboratory Practice for Nonclinical Laboratory Studies

The Food and Drug Administration (FDA) is seeking comment on whether to amend the regulations governing good laboratory practices (GLPs). The Agency decided that to require a GLP quality system for all facilities/laboratories, as well as to more completely address nonclinical studies as they are presently conducted, the Agency would need to modify the existing regulations.

Source: Federal Register — Health and Human ServicesOpen original release →