Compact Regs CFR 21
Author | : Food and Drug Administration Staff |
Publisher | : |
Total Pages | : 26 |
Release | : 2004-11 |
Genre | : |
ISBN | : 9780849318269 |
Download Compact Regs Cfr 21 full books in PDF, epub, and Kindle. Read online free Compact Regs Cfr 21 ebook anywhere anytime directly on your device. Fast Download speed and no annoying ads. We cannot guarantee that every ebooks is available!
Author | : Food and Drug Administration Staff |
Publisher | : |
Total Pages | : 26 |
Release | : 2004-11 |
Genre | : |
ISBN | : 9780849318269 |
Author | : Food and Drug Administration Staff |
Publisher | : Interpharm CRC |
Total Pages | : 58 |
Release | : 2004-11 |
Genre | : |
ISBN | : 9780849318320 |
Author | : Food and Drug Administration |
Publisher | : CRC Press |
Total Pages | : 115 |
Release | : 2001-12-31 |
Genre | : Medical |
ISBN | : 1135489807 |
The Compact Regs series provides full-text, pocket-sized format (3 3/4 inch x 5 1/2 inch) verbatim reproductions of key US FDA regulations. The texts are complete and have not been altered in any manner from the original sources. They are the perfect low-cost tools for: employees as part of documented GMP training programs, for suppliers/vendors so
Author | : Food and Drug Administration |
Publisher | : CRC Press |
Total Pages | : |
Release | : 2001-12-31 |
Genre | : Medical |
ISBN | : 9780849318306 |
The Compact Regs series provides full-text, pocket-sized format (3 3/4 inch x 5 1/2 inch) verbatim reproductions of key US FDA regulations. The texts are complete and have not been altered in any manner from the original sources. They are the perfect low-cost tools for: employees as part of documented GMP training programs, for suppliers/vendors so that they may provide components, labels, and parts with an understanding of FDA requirements, and for each clinical investigator, nurse, and technician to help assure compliance to clinical trial protocols. A keyword index can be found at the end of each booklet.
Author | : Interpharm |
Publisher | : CRC Press |
Total Pages | : 228 |
Release | : 2003-11-17 |
Genre | : Technology & Engineering |
ISBN | : 9781439828472 |
Supplemented with a convenient keyword index, this book provides a pocket-sized verbatim reproduction of key US FDA regulations. It presents the requirements as set forth by the FDA CFR 21 Parts 807, 812, and 814 to sell or distribute medical devices, including the pre-market approval requirements for the devices. The easy-to-use format that puts the exact section of the reg required by medical device manufacturers within easy reach. This is the perfect low-cost tool for employees as part of documented training programs; suppliers/vendors so that they may provide components, labels, and parts with an understanding of FDA requirements; and technicians charged with ensuring adherence to US FDA regulations.
Author | : Interpharm |
Publisher | : CRC Press |
Total Pages | : 68 |
Release | : 2003-11-17 |
Genre | : Technology & Engineering |
ISBN | : 9781439828489 |
This book presents Current Good Manufacturing Practice (CGMP) requirements as set forth by the FDA. Supplemented with a handy keyword index, it provides, in a pocket-sized format, the complete and unaltered text of CFR Part 820. The index at the end of the book helps readers find the exact section of the reg they need. The comb binding makes it easy to use and the 3 3/4 inch by 5 1/2 inch size makes it easy to take from the desk top to the shop floor. It is a cost-effective tool for use in documented GMP training programs, for suppliers and vendors who need to be FDA compliant, and technicians who must secure adherence to US FDA regulations.
Author | : Interpharm |
Publisher | : CRC Press |
Total Pages | : 241 |
Release | : 2013-10-23 |
Genre | : Medical |
ISBN | : 1482207982 |
This publication contains a verbatim reproduction of 21 CFR Part 50 Protection of Human Subjects, 21 CFR Part 54 Financial Disclosure by Clinical Investigators, 21 CFR Part 56 Institutional Review Boards & 21 CFR Part 312 Investigational New Drug Application.
Author | : Food and Drug Administration |
Publisher | : CRC Press |
Total Pages | : 54 |
Release | : 2002-09-30 |
Genre | : Medical |
ISBN | : 1135489661 |
The Compact Regs series provides full-text, pocket-sized format (3 3/4 inch x 5 1/2 inch) verbatim reproductions of key US FDA regulations. The texts are complete and have not been altered in any manner from the original sources. They are the perfect low-cost tools for: employees as part of documented GMP training programs, for suppliers/vendors so
Author | : Interpharm |
Publisher | : CRC Press |
Total Pages | : 36 |
Release | : 2003-11-17 |
Genre | : Technology & Engineering |
ISBN | : 1420025813 |
Supplemented with a handy keyword index, the Compact Regs series provides pocket-sized format (3 3/4 inch x 5 1/2 inch) verbatim reproductions of key US FDA regulations. The text is complete and has not been altered in any manner from the original source. Compact Regs Parts 110 and 111 covers good manufacturing practices for acid foods and batters. It describes prepackaging heat treatment of foodstuffs for a sufficient time and at a sufficient temperature to partially or completely inactivate the naturally occurring enzymes and effect other physical or biochemical changes in the food. It covers critical control points in a food process where there is a high probability that improper control may cause, allow, or contribute to a hazard or to filth in the final food, or decomposition of the final food. In short, the book covers food safety in food processing and manufacturing from the field to packaging and storage. This is the perfect low-cost tool for: employees as part of documented GMP training programs; suppliers/vendors so that they may provide components, labels, and parts with an understanding compliant with FDA requirements; and technicians charged with ensuring adherence to US FDA regulations.
Author | : Food and Drug Administration |
Publisher | : CRC Press |
Total Pages | : 201 |
Release | : 2002-09-30 |
Genre | : Medical |
ISBN | : 1135489734 |
The Compact Regs series provides full-text, pocket-sized format (3 3/4 inch x 5 1/2 inch) verbatim reproductions of key US FDA regulations. The texts are complete and have not been altered in any manner from the original sources. They are the perfect low-cost tools for: employees as part of documented GMP training programs, for suppliers/vendors so