Zdrowie i gospodarka · 30/04/2001

FDA Seeks Public Comment on Proposed GLP Regulations for Nonclinical Laboratory Studies

The Food and Drug Administration (FDA) is seeking public comment on proposed regulations for Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies, as mandated by the Paperwork Reduction Act of 1995. The agency is required to publish a 60-day notice in the Federal Register to allow for public input.