Zdrowie i gospodarka · 20/07/2001

FDA Submits Information Collection for OMB Review and Clearance

The Food and Drug Administration (FDA) has submitted a proposal for the collection of information related to Good Laboratory Practices (GLP) Regulations for Nonclinical Laboratory Studies to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.