GLP Testing Plan
AIRID operates a fully traceable GLP system in which product testing is systematically documented from receipt of test items through study conduct to final archiving. Records for each stage are securely maintained to ensure full traceability and compliance.
GLP organizational structure
Facility Manager
Overall responsibility for the GLP test facility, including resources, infrastructure, staff competency, and compliance with GLP requirements.
Study Directors
Single-point responsibility for the scientific conduct, integrity, and reporting of individual GLP studies.
Quality Assurance (QA) Managers
Independent oversight of GLP compliance through inspections, audits, and review of study documentation, with formal QA statements.
Archivist
Secure storage, indexing, retrieval, and long-term preservation of GLP records, ensuring data integrity and traceability.
Operational Teams (Laboratory, Semi-Field, Field)
Conduct experimental activities in accordance with approved study plans, SOPs, and quality requirements.