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Introduction to toxicological screen...

Chidambaram, Saravana Babu.

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Introduction to toxicological screening methods and good laboratory practice

Record Type:	Electronic resources : Monograph/item
Title/Author:	Introduction to toxicological screening methods and good laboratory practice/ by Saravana Babu Chidambaram, M. Mohamed Essa, M. Walid Qoronfleh.
Author:	Chidambaram, Saravana Babu.
other author:	Essa, M. Mohamed.
Published:	Singapore :Springer Singapore : : 2022.,
Description:	xx, 189 p. :ill., digital ;24 cm.
[NT 15003449]:	Chapter 1. Introduction to Toxicology -- Chapter 2. Laboratory Animal models -- Chapter 3. Toxicology Screening Methods -- Chapter 4. Toxicokinetics -- Chapter 5. Safety Pharmacology -- Chapter 6. Good Laboratory Practice.
Contained By:	Springer Nature eBook
Subject:	Toxicology - Laboratory manuals. -
Online resource:	https://doi.org/10.1007/978-981-16-6092-4
ISBN:	9789811660924

Introduction to toxicological screening methods and good laboratory practice
Chidambaram, Saravana Babu.

Introduction to toxicological screening methods and good laboratory practice[electronic resource] /by Saravana Babu Chidambaram, M. Mohamed Essa, M. Walid Qoronfleh. - Singapore :Springer Singapore :2022. - xx, 189 p. :ill., digital ;24 cm.

Chapter 1. Introduction to Toxicology -- Chapter 2. Laboratory Animal models -- Chapter 3. Toxicology Screening Methods -- Chapter 4. Toxicokinetics -- Chapter 5. Safety Pharmacology -- Chapter 6. Good Laboratory Practice.

This book focuses on the principles, methods, and interpretation involved in establishing the safety, risk, and hazard assessment of small molecules. It presents the regulatory requirements for risk and hazard identification as per the guidelines of the Organization for Economic Cooperation and Development (OECD), Paris, and the International Council for Harmonisation (ICH) of Technical Requirements for Pharmaceuticals for Human Use ICH and Schedule 'Y', India. It serves as reference material for undergraduate and postgraduate pharmacy degree students as well as senior researchers to learn about the principles, methods, and interpretations of systemic dosage (acute and repeated dose) and genotoxicity (in vitro and in vivo), special toxicological investigations such as reproductive and developmental toxicology, carcinogenicity, and toxicokinetics using animal models or in vitro methods, as applicable. This book is the first of its kind in providing information on the principles and methods of implementation of Good Laboratory Practice based on the guidelines of OECD. It includes detailed chapters about the regulatory requirements and guidelines in pharmaceutical products and agrochemicals. It also describes the infrastructure needed for preclinical studies, including in vivo and in vitro facilities.

ISBN: 9789811660924

Standard No.: 10.1007/978-981-16-6092-4doiSubjects--Topical Terms:

3565842
Toxicology
--Laboratory manuals.

LC Class. No.: RA1211 / .C45 2022

Dewey Class. No.: 615.90072

Introduction to toxicological screening methods and good laboratory practice
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245 1 0 $a Introduction to toxicological screening methods and good laboratory practice $h [electronic resource] / $c by Saravana Babu Chidambaram, M. Mohamed Essa, M. Walid Qoronfleh.
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505 0 $a Chapter 1. Introduction to Toxicology -- Chapter 2. Laboratory Animal models -- Chapter 3. Toxicology Screening Methods -- Chapter 4. Toxicokinetics -- Chapter 5. Safety Pharmacology -- Chapter 6. Good Laboratory Practice.
520 $a This book focuses on the principles, methods, and interpretation involved in establishing the safety, risk, and hazard assessment of small molecules. It presents the regulatory requirements for risk and hazard identification as per the guidelines of the Organization for Economic Cooperation and Development (OECD), Paris, and the International Council for Harmonisation (ICH) of Technical Requirements for Pharmaceuticals for Human Use ICH and Schedule 'Y', India. It serves as reference material for undergraduate and postgraduate pharmacy degree students as well as senior researchers to learn about the principles, methods, and interpretations of systemic dosage (acute and repeated dose) and genotoxicity (in vitro and in vivo), special toxicological investigations such as reproductive and developmental toxicology, carcinogenicity, and toxicokinetics using animal models or in vitro methods, as applicable. This book is the first of its kind in providing information on the principles and methods of implementation of Good Laboratory Practice based on the guidelines of OECD. It includes detailed chapters about the regulatory requirements and guidelines in pharmaceutical products and agrochemicals. It also describes the infrastructure needed for preclinical studies, including in vivo and in vitro facilities.
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