Good Laboratory Practice (GLP) is a quality system ensuring the uniformity, consistency, reliability, and integrity of non-clinical laboratory safety studies. Its primary objective is to guarantee data validity for regulatory hazard assessments, with clear learning outcomes covering compliance, safety, and quality assurance.
Created by Dr. YASSER MEKKY
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Join Now| # | Content |
|---|---|
| 1 | • Introduction and history of GLP regulations. |
| 2 | • Organization and personnel responsibilities. |
| 3 | • Quality Assurance Unit (QAU) role and audits. |
| 4 | • Facilities, equipment, and calibration maintenance. |
| 5 | • Handling test and reference items. |
| 6 | • Standard Operating Procedures (SOPs) creation. |
| 7 | • Study protocol design and execution. |
| 8 | • Data recording, reporting, and archiving. |
| # | Outcomes |
|---|---|
| • Understand core GLP principles and regulatory frameworks. | |
| • Design and manage compliant experimental studies. | |
| • Maintain accurate records, data trails, and specimen tracking. | |
| • Identify and mitigate laboratory safety and quality risks. |
| # | Participants |
|---|---|
| 1 |
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• Laboratory Directors and Management
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| 2 |
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• Study Directors and Principal Investigators
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| 3 |
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• Quality Assurance (QA) Personnel
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| 4 |
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• Laboratory Technicians and Researchers
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601, El Horeya St,7th floor Zizinia, Alexandria, Egypt
(+2) 01099 770 699
dr.yassermekky@charismaqs.com
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