GLP 0: Good Laboratory Practice, Overview

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Program/Course ID: GLPRA Enrollment Period: 12 months. Average Learning Time: ~. Additional Resources: Supplemental materials & activities. Credit Hours: 3 credits. Method of Training: Online, asynchronous, self-paced eLearning. Accessibility: 24/7 access to all program materials. Demonstration: Four (4) free trial courses are available. Group/Employee Training: Click here to request a quote or invoice. Final Assessment: Multiple choice; unlimited attempts. Certificate: Encrypted PDF with QR validation code.

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Saturday, May 16, 2026 UPDATE:
This program is currently unavailable for enrollment.
It may have been updated or discontinued.
Check for newer version in our catalog.

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Outline: INTRODUCTION 1. Course Information 2. Interface Tour 3. Course Overview PURPOSE AND ELEMENTS OF GLP 4. Objectives 5. Pre-Test 6. Origins of the GLP Regulations 7. Protocols and Reports 8. Quality Assurance Program 9. Inspections of GLP Labs 10. Progress Check GLP RESPONSIBILITIES 11. Objectives 12. Pre-Test 13. Responsibilities of Management and Personnel 14. Responsibilities of the Study Director 15. Responsibilities of Quality Assurance 16. Progress Check AREAS OF GLP 17. Objectives 18. Pre-Test 19. Facilities and Instrumentation 20. Reagents and Solutions 21. Animal Care 22. Test and Control Materials 23. Progress Check DOCUMENTATION 24. Objectives 25. Pre-Test 26. Standard Operating Procedures 27. Document Change Control 28. Data Recording Rules 29. Records/Archive Management 30. Progress Check CONCLUSION 31. Summary		Objectives: List the purpose of Good Laboratory Practice (GLP) regulations. Describe two events that inform the institution of the GLP regulations. Describe four elements of GLP. Discuss the three areas that will be reviewed during a GLP inspection. List the responsibilities of Management. Understand Personnel responsibilities. Describe the responsibilities of the Study Director. Discuss the responsibilities of Quality Assurance. Understand the GLP area of Facilities and Instrumentation. Describe Standard Operating Procedures. Discuss the GLP area of Reagents and Solutions. Understand the GLP area of Animal Care. Describe the GLP area of Test and Control Materials. Describe the purpose of SOPs and document change control. List the records required under GLP. List the data recording rules intended to demonstrate the integrity of nonclinical study data. Describe the retention period for GLP study data.

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