1.7 Good Laboratory Practice (GLP): Key Requirements
1.7 Good Laboratory Practice (GLP): Key Requirements contains 4 topic pages in Phase 1 — Introduction to Pharmacological Research & Regulatory Framework.
Topic Group
Topics
Continue through the related topic pages.
1.7.1 What is GLP?
Good Laboratory Practice is a formal quality-management system governing the organisational process and conditions under which non-clinical health and...
1.7.2 Essential Elements of a GLP System
**Test facility organisation:** Standard Operating Procedures govern all operations, and a Quality Assurance unit operates independently of the...
1.7.3 GLP Documentation
Documentation is the operational backbone of any GLP system, since a study that is not fully and contemporaneously documented cannot, in the eyes of a...
1.7.4 GLP Applications
GLP principles are applied specifically to non-clinical safety studies whose data are destined for regulatory submission: acute, sub-acute, sub-chronic, and...