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Good Laboratory Practice: Nonclinical Laboratory Studies Concise Reference
Contributor(s): Allport-Settle, Mindy J. (Author)
ISBN: 0983071918     ISBN-13: 9780983071914
Publisher: Pharmalogika
OUR PRICE:   $35.14  
Product Type: Paperback
Published: October 2010
Qty:
Additional Information
BISAC Categories:
- Medical | Biotechnology
Physical Information: 0.58" H x 6" W x 9" (0.82 lbs) 276 pages
 
Descriptions, Reviews, Etc.
Publisher Description:
This book is designed to be a unified reference source for the U.S. Food and Drug Adminstration's Good Laboratory Practice regulations, guidance, and associated documents for pharmaceutical, biologics and medical device products nonclinical trials. Good Laboratory Practice Regulations and Guidance: * FDA Overview and Orientation * Overview of GCP and Introduction to GLP * Part I: Federal Regulations Relating to Good Laboratory Practice o Parts 58: Good Laboratory Practice for Nonclinical Laboratory Studies o 1987 Final Rule - Good Laboratory Practice Regulations * Part II: Guidance Documents o Bioresearch Monitoring Good Laboratory Practice o Good Laboratory Practices Questions and Answers * Part III: Redbook 2000 o IV.B.1 General Guidelines for Designing and Conducting Toxicity Studies o IV.B.2 Guidelines for Reporting the Results of Toxicity Studies Reference Tools * Part IV: Combined Glossary and Index