Zdrowie i gospodarka · 12/03/2008
FDA Requests Public Comment on Proposed Good Laboratory Practice Regulations for Nonclinical Studies
The Food and Drug Administration (FDA) is seeking public input on proposed regulations for good laboratory practice (GLP) in nonclinical laboratory studies, as required by the Paperwork Reduction Act of 1995.
Source: Federal Register — Food and Drug AdministrationOpen original release →