GLP Certification in Jordan:

GLP Certification Process in Jordan

GLP certification begins with a comprehensive gap assessment benchmarking laboratory operations against OECD Good Laboratory Practice Principles to identify compliance gaps. Laboratories then develop foundational documentation, including a GLP Quality Manual defining policies, Standard Operating Procedures (SOPs) for all critical activities, and standardized study plan templates. An independent Quality Assurance (QA) unit is established to ensure unbiased oversight of studies and systems.

Implementation follows through staff training, internal audits, and mock inspections. Laboratories then apply to inspection body for official review and undergo an inspection evaluating facilities, systems, and raw data. Any nonconformities are addressed through corrective actions, after which GLP recognition is granted, subject to periodic surveillance inspections.

Key GLP Requirements

• Organizational structure: Clearly defined management responsibilities, adequate skilled personnel, and segregated facilities to prevent cross-contamination.
• Independent QA: Autonomous QA program conducting routine inspections, audits, and report verification, reporting directly to top management.
• Study Director accountability: Single responsible authority for study execution, deviations, data integrity, and final reports.
• SOPs & documentation: Version-controlled, approved procedures for all activities, with documented staff training and competency verification.
• Equipment management: Traceable calibration, validation, and maintenance of instruments; proper characterization and stability of test and reference items.
• Data handling: Contemporaneous and accurate data recording, with secure, retrievable archiving for a minimum 10-year retention.
• Computerized systems: Fully validated systems with access controls and audit trails to ensure ALCOA+ data integrity compliance.

Timeline Expectations

Small to mid-size laboratories typically complete GLP certification within 2–6 months, supported by faster documentation and training cycles. Larger, multi-study operations may require 6–9 months, factoring in extensive system validations and infrastructure enhancements. Timelines vary based on initial readiness, inspection scheduling, and corrective action closure. With proactive consulting, timelines can often be reduced by 20–30%.

Common GLP Challenges in Jordan

Jordanian laboratories commonly face shortages of trained independent QA professionals, often requiring recruitment or intensive upskilling in hubs such as Amman and Irbid. Documentation inconsistencies persist due to legacy paper-based systems lacking change control. Data integrity risks arise from unvalidated software vulnerable to unauthorized changes, while limited GLP exposure among technical staff shifts focus toward research rather than compliance. Resource constraints in smaller facilities further extend implementation timelines.

Why Choose Vertex Certifiers?

Vertex Certifiers delivers OECD-aligned GLP expertise, guiding Jordanian laboratories end-to-end from initial audits to final approval. Our services include ready-to-use SOP kits, robust QA frameworks, staff training, and mock inspections that closely simulate JAB/JFDA scrutiny. With flexible remote and onsite consulting models and milestone-driven pricing, we ensure timelines, budgets, and compliance goals align for rapid return on investment.

Conclusion

GLP certification strengthens Jordanian laboratories by enhancing regulatory credibility, data reliability, and global collaboration opportunities. By operating under harmonized OECD principles, laboratories unlock export potential and long-term growth across pharmaceutical, chemical, and agrochemical sectors.