Course Information
The OECD principles of Good Laboratory Practice (GLP) sets out the requirements for the management of non-clinical studies and it provides standardization on the planning, recording, reporting, and monitoring processes within the organizations. The compilation of a GLP dossier is part of the required regulatory submission.
This course has been designed for laboratory professionals and regulatory affairs professionals from analytical, testing, diagnostics and other laboratories to deepen and strengthen their skills and knowledge in implementing OECD Principles of Good Laboratory Practice in their workplace.
Learning Outcomes
- Resources: Organization, personnel, facilities and equipment
- Characterization: Test items and test systems
- Rules: Protocols, standard operating procedures (SOPs)
- Results: Raw data, final report and archives
- Quality Assurance: Independent monitoring of research processes
- Performing GLP study
Course
Schedule
Lesson Plan
This course consists of 1 modules:
This course will deepen and strengthen participants’ skills and knowledge in implementing OECD Principles of Good Laboratory Practice in their workplace.
Certification
A Certificate of Performance will be awarded to participants who achieve at least 75% attendance and pass all required assessment(s).
Course Fees
| Applicants / Eligibility | Fees |
|---|---|
| Singapore Citizens (SC) below the age of 40 years | $166.92 |
| Singapore Citizens (SC) aged 40 and above | $62.92 |
| Singapore Permanent Residents (PR) | $166.92 |
| Enhanced Training Support for SME Scheme (for SC & SPR) | $62.92 |
| Others (and Repeat Students) | $556.40 |
| Full Course Fee (Before GST) | $520.00 |