After more than twenty years of use Good Laboratory Practice, or GLP, has attained a secure place in the world of testing chemicals and other "test items" with regard to their safety for humans and the environment. Gone are the days when the GLP regulations were hotly debated amongst scientists in academia and industry and were accused of stifling flexibility in, imaginative approaches to, and science-based conduct of, all kinds of studies concerned with toxic effects and other parameters important for the evaluation and assessment of products submitted for registration and permission to market. The GLP regulations have developed from rules on how to exactly document the planning, conduct and reporting of toxicity studies to a quality system for the management of a multitude of study types, from the simple determination of a physical/chemical parameter to the most complex field studies or ecotoxicology studies. At the same time the term "Good Laboratory Practice" has become somewhat of a slogan with the aim to characterise any reliably conducted laboratory work.

I. What is Good Laboratory Practice All About?- 1. Introduction

2. The History of GLP
2.1 The Early Days and the Causative Events
2.2 The First Regulations
2.3 International Ripples: The OECD Principles
2.4 The Principles and Their Interpretation
2.5 Closing the Circle? - The Detection of Test Item in Control Samples
3. The Idea Behind GLP
4. The Areas of Application
5. The Pillars of Good Laboratory Practice
6. Where Can GLP be Profitably Applied?- 7. GLP and Other Laboratory Quality Systems
II. How is Good Laboratory Practice Regulated?- 1. Introduction
2. Definitions in GLP
2.1 Good Laboratory Practice
2.2 Management
2.3 Study Director and Principal Investigator
2.4 Test Facility and Test Site
2.5 The Study
2.6 Short-Term Studies
2.7 Initiation, Starting and Completion Dates
2.8 Study Plan, Amendments and Deviations
2.9 Raw Data 94
2.10 The Phases of a Study
2.11 The Master Schedule
2.12 Test and Reference Item
2.13 Additional Definitions
3. Responsibilities in Good Laboratory Practice
3.1 Management
3.2 Study Director and Principal Investigator
3.3 Study Personnel
3.4 The Sponsor
4. The Quality Assurance Programme
4.1 General Considerations
4.2 Quality Assurance Inspections
4.3 Quality Assurance Inspection Reports
4.4 Audits of Raw Data and of Final Reports
4.5 The Quality Assurance Statement
5. Facilities
5.1 General Requirements
5.2 Test System Facilities
5.3 Facilities for Handling Test and Reference Items
5.4 Archive Facilities
6. Apparatus, Materials and Reagents
7. Computerised Systems
7.1 Introduction
7.2 Basic Considerations
7.3 Data considerations
7.4 Prospective Validation
7.5 Retrospective Evaluation
7.6 Maintenance and Change Control
7.7 Security
7.8 Levels of Complexity
8. Test Systems
8.1 Physical/Chemical Test Systems
8.2 Biological Test Systems
9. Test and Reference Items
9.1 Handling andDocumentation
9.2 Characterisation
9.3 Expiry Dates
9.4 Sample Retention
10. Standard Operating Procedures
10.1 Introduction
10.2 The Format
10.3 Issue, Approval and Distribution
10.4 On-line SOPs
10.5 The Content
10.6 Where are SOPs required?- 11. Study Performance and Reporting
11.1 The Study Plan
11.2 Study Conduct
11.3 The Final Report
11.4 Re-opening and Amending a Study
11.5 Discontinued Studies
12. The Archives
12.1 Storage Period
12.2 Indexing and Retrieval
12.3 Security
12.4 Archiving of Electronic Raw Data
12.5 Archive location, merging and dissolution
III. How can Good Laboratory Practice be Introduced in a Test Facility?- 1. Introduction
2. General Aspects
3. A General Way to Implementation
3.1 The preliminaries
3.2 The organisation
3.3 Separation and distribution of facilities and equipment
3.4 Interlude: Personnel documentation
3.5 Distributing Responsibilities
3.6 The Major Task: Standard Operating Procedures
3.7 Second Interlude: Quality Assurance and IT
3.8 The Personnel: Education and Training
3.9 Study Plans
3.10 Test and Reference Item Issues
3.11 Study Conduct
IV. How is Compliance with Good Laboratory Practice Monitored?- 1. Introduction
2. National Monitoring Authorities
3. MOUs, MRAs, and MJVs.