Course Overview
Good Laboratory Practices (GLP) are internationally accepted standards designed to ensure the quality, integrity, and reliability of non-clinical laboratory studies. GLP principles apply to pharmaceutical, biotech, agrochemical, food, cosmetics, and environmental testing laboratories that generate data for regulatory submissions. This GLP Training Course is carefully designed to provide complete knowledge on compliance-based laboratory operations, documentation standards, audit readiness, and ethical scientific practices. The course builds strong foundational understanding of how laboratories function under strict regulatory frameworks. Learners gain practical knowledge of laboratory design, instrument qualification, sample handling, calibration procedures, validation documentation, and safety programs. The focus is on maintaining traceable, accurate, and defendable data that regulators can trust. Through real case discussions, you will understand how simple errors in documentation, sampling, and data recording can lead to major non-compliances. You will also learn about study planning, protocol preparation, SOP writing, and report finalization to support regulatory submissions such as to OECD, US-FDA, EMA, and other authorities.
This training prepares individuals to work confidently in GLP-compliant labs including R&D laboratories, analytical and microbiology labs, CROs, toxicology facilities, environmental testing centers, and pharmaceutical QC labs. The course ensures that every learner becomes capable of maintaining laboratory operations with accountability, integrity, and scientific accuracy.
Who Should Enroll
QC & QA professionals in testing laboratories
Lab analysts, technicians, and supervisors
R&D scientists in pharma, biotech, food, and cosmetics
Environmental and chemical testing professionals
Students in life sciences seeking lab-based careers
Anyone preparing for GLP audits and regulatory inspections
What You'll Learn
Training aligned with OECD GLP, WHO, USFDA, and NABL
requirements
Practical demonstration of lab workflows and documentation
Trainer guidance from industry-experienced quality professionals
Includes SOP samples, data recording templates, and audit checklist
Certificate of Completion to enhance career opportunities
Improves laboratory compliance and job readiness
Prerequisites
Introduction to GLP and
its regulatory background
Laboratory organization, roles, and responsibilities
Equipment qualification, calibration, and maintenance
Sample management, chain-of-custody, and traceability
Good Documentation Practices (GDP) and data integrity
Analytical method execution and result reporting
Chemical handling, MSDS knowledge, and lab safety
Internal audits, deviations, CAPA, and quality systems
Study planning, raw data handling, and archiving procedures
Handling GLP inspections and common non-compliances
Curriculum
Detailed curriculum information will be available soon.
Course Format
This course offers a comprehensive learning experience with interactive content.
Course Materials
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