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The Indispensable Guide to Good Laboratory Practice ( GLP )

The Indispensable Guide to Good Laboratory Practice ( GLP ) [Kindle Edition]

Mark G. Slomiany

Kindle-Preis: EUR 3,55 Inkl. MwSt. und kostenloser drahtloser Lieferung über Amazon Whispernet

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Taschenbuch EUR 6,70  



Familiarity with Good Laboratory Practice (GLP) is a necessity for those working in or aspiring to work in biotech, pharma, and even academic research, where partnerships with industry require ever greater awareness of drug development regulations. Thus, this guidebook serves to not only summarize GLP regulations, but explain the interaction of these various components in the development of a GLP compliant study. Far from being long-winded, special attention has been paid to the brevity of each chapter. If more detail is needed, the reader can easily refer to the official FDA verbiage (CFR 21, Part 58) provided below each chapter summary.

Inspired by the lack of affordable, succinct, and easily accessible training options available to students, scientists, and entrepreneurs, Dr. Slomiany set out to create a guidebook which conveys the underlying principles of GLP in an easily digestible format, while providing resources for more in-depth study.

Though presented in kindle format, this document can easily be opened on a standard web browser or word processing program.



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Die hilfreichsten Kundenrezensionen auf (beta) 3.0 von 5 Sternen  3 Rezensionen
8 von 8 Kunden fanden die folgende Rezension hilfreich
5.0 von 5 Sternen Well Written 30. Oktober 2009
Von Vickie - Veröffentlicht auf
Format:Kindle Edition
After reading this book, the process of Good Laboratory Practice (GLP) did not seem as daunting as previously perceived from reading other more complex and technical references. This book is well written and succinct in that anyone who reads will understand the principles and process of GLP. The author went to great lengths to explain the requirements and processes in a manner that is not intimidating and one is left feeling that GLP process in whatever laboratory setting or field experiment is attainable. The glossary was most helpful to me as it explains the terms used in a GLP process, what exactly is an SOP and the differences in an SOP and a Protocol.
2.0 von 5 Sternen Save your money 10. Juli 2013
Von Miguel - Veröffentlicht auf
Format:Taschenbuch|Von Amazon bestätigter Kauf
This book skims through many important aspects of GLP, and is more of an outline. I would not recommend this book to anyone.
2.0 von 5 Sternen Very. Very. Very. Brief. 3. August 2012
Von Kanga - Veröffentlicht auf
Format:Taschenbuch|Von Amazon bestätigter Kauf
I was a bit surprised when I got this "book". I would have called it a pamplet, or perhaps an article.

It is nominally 66 pages, but the actual stuff you want covers just 62 pages of that (page 5 to page 66). The font appears large and the line spacing (just 5 lines per inch) seems large. The pages seem undersized (8" x 10") and the margins seem wide (1" all around). You can see what this means - less actual content.

The author has summarized the requirements of the various chapters of the CFR - mostly in outline or bullet format following the pattern of the CFR. I didn't find it any easier than reading the actual CFR and leaves you worrying if you (or the author) missed something that appears in the actual CFR's.

Another reviewer made positive comments about the glossary. I found no glossary in the book I purchased - don't know whether that existed in an earlier version or what.
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the objective is not only quality of data but also traceability and integrity of data, &quote;
Markiert von 3 Kindle-Nutzern
GLPs regulate all non-clinical safety studies that support or are intended to support applications for research or marketing permits for products regulated by the &quote;
Markiert von 3 Kindle-Nutzern

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