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| Title: | Introduction to Toxicological Screening Methods and Good Laboratory Practice |
|---|---|
| From: |
by Saravana Babu Chidambaram, M. Mohamed Essa, M. Walid Qoronfleh.
|
| Person: |
Chidambaram, Saravana Babu.
author. aut http://id.loc.gov/vocabulary/relators/aut Essa, M. Mohamed. Qoronfleh, M. Walid. |
| Main Authors: | , , |
| Corporate Author: | |
| Format: | Electronic eBook |
| Language: | English |
| Published: |
Singapore :
Springer Nature Singapore : Imprint: Springer,
2022.
|
| Edition: | 1st ed. 2022. |
| Subjects: | |
| Online Access: | https://doi.org/10.1007/978-981-16-6092-4 |
| Summary: | 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. |
| Physical Description: | 1 Online-Ressource (XX, 189 p. 1 illus.) |
| ISBN: | 9789811660924 |
Staff View
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| 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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| contents | 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. |
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| spelling | Chidambaram, Saravana Babu. author. aut http://id.loc.gov/vocabulary/relators/aut Introduction to Toxicological Screening Methods and Good Laboratory Practice [electronic resource] / by Saravana Babu Chidambaram, M. Mohamed Essa, M. Walid Qoronfleh. 1st ed. 2022. Singapore : Springer Nature Singapore : Imprint: Springer, 2022. 1 Online-Ressource (XX, 189 p. 1 illus.) text txt rdacontent computer c rdamedia online resource cr rdacarrier text file PDF rda 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. Toxicology. Pharmacology. Medical sciences. Drug development. Pharmacy. Pharmaceutical chemistry. Preclinical Research. Pharmaceutics. Essa, M. Mohamed. author. aut http://id.loc.gov/vocabulary/relators/aut Qoronfleh, M. Walid. author. aut http://id.loc.gov/vocabulary/relators/aut SpringerLink (Online service) Springer Nature eBook Printed edition: 9789811660917 Printed edition: 9789811660931 Printed edition: 9789811660948 |
| spellingShingle | Chidambaram, Saravana Babu Essa, M. Mohamed Qoronfleh, M. Walid Introduction to Toxicological Screening Methods and Good Laboratory Practice 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. Toxicology. Pharmacology. Medical sciences. Drug development. Pharmacy. Pharmaceutical chemistry. Preclinical Research. Pharmaceutics. |
| title | Introduction to Toxicological Screening Methods and Good Laboratory Practice |
| title_auth | Introduction to Toxicological Screening Methods and Good Laboratory Practice |
| title_exact_search | Introduction to Toxicological Screening Methods and Good Laboratory Practice |
| title_full | Introduction to Toxicological Screening Methods and Good Laboratory Practice [electronic resource] / by Saravana Babu Chidambaram, M. Mohamed Essa, M. Walid Qoronfleh. |
| title_fullStr | Introduction to Toxicological Screening Methods and Good Laboratory Practice [electronic resource] / by Saravana Babu Chidambaram, M. Mohamed Essa, M. Walid Qoronfleh. |
| title_full_unstemmed | Introduction to Toxicological Screening Methods and Good Laboratory Practice [electronic resource] / by Saravana Babu Chidambaram, M. Mohamed Essa, M. Walid Qoronfleh. |
| title_short | Introduction to Toxicological Screening Methods and Good Laboratory Practice |
| title_sort | introduction to toxicological screening methods and good laboratory practice |
| topic | Toxicology. Pharmacology. Medical sciences. Drug development. Pharmacy. Pharmaceutical chemistry. Preclinical Research. Pharmaceutics. |
| topic_facet | Toxicology. Pharmacology. Medical sciences. Drug development. Pharmacy. Pharmaceutical chemistry. Preclinical Research. Pharmaceutics. |
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