Congressional Record
Author : United States. Congress
Publisher :
Page : 1324 pages
File Size : 45,57 MB
Release : 1968
Category : Law
ISBN :
Author : United States. Congress
Publisher :
Page : 1324 pages
File Size : 45,57 MB
Release : 1968
Category : Law
ISBN :
Author :
Publisher :
Page : 8 pages
File Size : 12,65 MB
Release : 2007
Category : Budget
ISBN :
Author : United States
Publisher :
Page : 6 pages
File Size : 40,43 MB
Release : 1998
Category : Administrative agencies
ISBN :
Author : United States. Congress. Senate
Publisher :
Page : 1176 pages
File Size : 46,5 MB
Release : 1978
Category : Legislation
ISBN :
Author : United States. Congress. House. Committee on Energy and Commerce
Publisher :
Page : 28 pages
File Size : 39,88 MB
Release : 2009
Category :
ISBN :
Author : Food and Drug Administration
Publisher :
Page : 0 pages
File Size : 22,99 MB
Release : 2003
Category : Drugs
ISBN : 9780865879737
Available now to FDA-regulated organizations, this manual allows facility managers to look at their operation's regulatory compliance through the eyes of the government. Because this is the primary reference manual used by FDA personnel to conduct field investigation activities, you can feel confident you are preparing appropriate planning or action. This manual includes revised instructions regarding the release of information and covers FDA's policies and expectations on a comprehensive range of topics: FDA's authority to enter and inspect, inspection notification, detailed inspection procedures, recall monitoring, inspecting import procedures, computerized data requests, federal/state inspection relationships, discussions with management regarding privileged information, seizure and prosecution, HACCP, bioengineered food, dietary supplements, cosmetics, bioterrorism, and product disposition. The manual also includes a directory of Office of Regulatory Affairs offices and divisions.
Author : Adam Schiff
Publisher :
Page : 304 pages
File Size : 22,10 MB
Release : 2019-12-03
Category : Political Science
ISBN : 9781680923117
Report of the House Permanent Select Committee on Intelligence, Pursuant to H. Res. 660 in Consultation with the House Committee on Oversight and Reform and the House Committee on Foreign Affairs This report reflects the evidence gathered thus far by the House Permanent Select Committee on Intelligence, in coordination with the Committee on Oversight and Reform and the Committee on Foreign Affairs, as part of the House of Representatives' impeachment inquiry into Donald J. Trump, the 45th President of the United States.
Author : United States Sentencing Commission
Publisher :
Page : 456 pages
File Size : 11,28 MB
Release : 1995
Category : Sentences (Criminal procedure)
ISBN :
Author : United States
Publisher :
Page : 1192 pages
File Size : 14,62 MB
Release : 1989
Category : Law
ISBN :
Author : Institute of Medicine
Publisher : National Academies Press
Page : 158 pages
File Size : 21,31 MB
Release : 1999-04-29
Category : Medical
ISBN : 0309184134
The Institute of Medicine's (IOM's) Food Forum was established in 1993 to allow science and technology leaders in the food industry, top administrators in the federal government, representatives from consumer interest groups, and academicians to discuss and debate food and food safety issues openly and in a neutral setting. The Forum provides a mechanism for these diverse groups to identify possible approaches for addressing food and food safety problems and issues surrounding the often complex interactions among industry, academia, regulatory agencies, and consumers. On May 6-7, 1997, the Forum convened a workshop titled Enhancing the Regulatory Decision-Making Process for Direct Food Ingredient Technologies. Workshop speakers and participants discussed legal aspects of the direct food additive approval process, changes in science and technology, and opportunities for reform. Two background papers, which can be found in Appendix A and B, were shared with the participants prior to the workshop. The first paper provided a description and history of the legal framework of the food ingredient approval process and the second paper focused on changes in science and technology practices with emphasis placed on lessons learned from case studies. This document presents a summary of the workshop.