Notices of Judgment Under the Federal Food, Drug, and Cosmetic Act
Author: United States. Food and Drug Administration
Publisher:
Published: 1940
Total Pages: 1378
ISBN-13:
DOWNLOAD EBOOKRead and Download eBook Full
Author: United States. Food and Drug Administration
Publisher:
Published: 1940
Total Pages: 1378
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Food and Drug Administration
Publisher:
Published: 1965
Total Pages: 38
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Food and Drug Administration
Publisher:
Published: 1949
Total Pages: 1762
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Food and Drug Administration
Publisher:
Published: 1943
Total Pages: 320
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Food and Drug Administration
Publisher:
Published: 1940
Total Pages: 1866
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Food and Drug Administration
Publisher:
Published: 1940
Total Pages: 186
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Federal Trade Commission. Bureau of Consumer Protection
Publisher:
Published: 1998
Total Pages: 32
ISBN-13:
DOWNLOAD EBOOKAuthor: United States. Food and Drug Administration
Publisher:
Published: 1938
Total Pages: 918
ISBN-13:
DOWNLOAD EBOOKAuthor: Institute of Medicine
Publisher: National Academies Press
Published: 1999-04-29
Total Pages: 158
ISBN-13: 0309184134
DOWNLOAD EBOOKThe 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.