Good Laboratory Practices (GLP) are a quality system for managing research laboratories and organizations to ensure uniformity, consistency, reliability and reproducibility in chemical safety testing. GLP aims to control non-clinical studies evaluating the safety of chemicals for humans, animals and the environment. Key aspects of GLP include defined principles, objectives, procedures and guidelines from organizations like the OECD and US FDA for conducting chemical safety tests.

1. GURU NANAK KHALSA COLLEGE
ANALYTICAL CHEMISTRY
BY
SHARMEEN KHAN

2. TOPIC
 GOOD LABORATORY PRACTICES
• PRINCIPLE,OBJECTIVE,OECD GUIDELINES,THE
US FDA 21CFR58,Klimisch score

3. CONTENT
• INTRODUCTION
• PRINCIPLE
• OBJECTIVE
• DEFINATIONS
• PROCEDURES
• CONCLUTION
• REFERENCES

4. INTRODUCTION
• In the experimental research arena, the phrase good
laboratory practice or GLP specifically refers to a quality
system of management.
• This system controls research laboratories and
organizations to try to ensure the uniformity, consistency,
reliability, reproducibility, quality, and integrity of chemical
non-clinical safety tests.
• GLP applies to non-clinical studies conducted for the
assessment of the safety or efficacy of chemicals to man,
animals and the environment.