Fish and Fishery Products
Title | Fish and Fishery Products PDF eBook |
Author | Barry Leonard |
Publisher | DIANE Publishing |
Pages | 476 |
Release | 2011-08 |
Genre | Technology & Engineering |
ISBN | 143798746X |
This guidance will assist processors of fish and fishery products in the development of their Hazard Analysis Critical Control Point (HACCP) plans. Processors of fish and fishery products will find info. that will help them identify hazards that are associated with their products, and help them formulate control strategies. It will help consumers understand commercial seafood safety in terms of hazards and their controls. It does not specifically address safe handling practices by consumers or by retail estab., although the concepts contained in this guidance are applicable to both. This guidance will serve as a tool to be used by fed. and state regulatory officials in the evaluation of HACCP plans for fish and fishery products. Illustrations. This is a print on demand report.
FDA Papers
Title | FDA Papers PDF eBook |
Author | |
Publisher | |
Pages | 454 |
Release | 1967 |
Genre | Consumer protection |
ISBN |
FDA Approved Animal Drug Products
Title | FDA Approved Animal Drug Products PDF eBook |
Author | |
Publisher | |
Pages | 144 |
Release | 1998 |
Genre | Veterinary drugs |
ISBN |
FDA Papers
Title | FDA Papers PDF eBook |
Author | |
Publisher | |
Pages | 892 |
Release | 1969 |
Genre | Consumer protection |
ISBN |
FDA Papers
Title | FDA Papers PDF eBook |
Author | |
Publisher | |
Pages | 438 |
Release | 1968 |
Genre | Consumer protection |
ISBN |
Dietary Supplements
Title | Dietary Supplements PDF eBook |
Author | United States. Federal Trade Commission. Bureau of Consumer Protection |
Publisher | |
Pages | 32 |
Release | 1998 |
Genre | Advertising |
ISBN |
Public Health Effectiveness of the FDA 510(k) Clearance Process
Title | Public Health Effectiveness of the FDA 510(k) Clearance Process PDF eBook |
Author | Institute of Medicine |
Publisher | National Academies Press |
Pages | 141 |
Release | 2010-10-04 |
Genre | Medical |
ISBN | 0309162904 |
The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its assessment of FDA's premarket clearance process for medical devices, the IOM held a workshop June 14-15 to discuss how to best balance patient safety and technological innovation. This document summarizes the workshop.