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Contact SupplierWhat is GLP Certification (OECD Principles, 2022)?
GLP stands for Good Laboratory Practice, a quality system defined under the OECD Principles of GLP (latest updated version 2022). It ensures that non-clinical laboratory studies—such as those related to pharmaceuticals, pesticides, cosmetics, chemicals, and food safety—are planned, performed, monitored, recorded, archived, and reported in a reliable and reproducible manner. GLP certification helps laboratories prove data integrity and compliance with international regulatory expectations.
GLP Certificate – Overview
GLP certification is essential for laboratories conducting safety testing of products for human health and the environment. It assures that the study data submitted to regulators are valid and scientifically sound. The OECD GLP Principles are globally recognized and implemented by regulatory authorities such as FDA, CDSCO, EPA, and others. This certification is often mandatory for labs seeking to participate in global supply chains or submit studies for product approval. Laboratories that follow GLP demonstrate commitment to transparency, accountability, and quality assurance.
GLP Key Requirements for Certification
Establish and document standard operating procedures (SOPs) for study conduct.
Maintain qualified and trained personnel for each critical function.
Ensure accurate equipment calibration, maintenance, and validation.
Implement proper sample collection, storage, and tracking mechanisms.
Maintain a robust quality assurance (QA) unit independent of operations.
Ensure data traceability through proper documentation and archiving.
Comply with ethical practices and provide access for regulatory audits.
Keep secure and well-defined test facilities with access control and contamination prevention.
GLP Consultancy and Implementation Support
At Growth Management Corporation, we provide end-to-end consultancy for GLP certification based on OECD 2022 Principles. Our team supports test facilities, R&D labs, CROs, and pharma companies with readiness assessments, SOP development, and documentation guidance. We help your team adopt GLP systems with practical tools and training. From setting up data management systems to staff competence building, we ensure your laboratory is audit-ready and aligned with international norms.
GLP Certification Process
Gap Analysis – Review current lab systems and processes against GLP requirements.
System Development – Draft policies, SOPs, forms, and records required for GLP compliance.
Training – Conduct hands-on training for QA, technical, and managerial staff.
Internal Audit – Perform pre-certification audits to assess preparedness.
Regulatory Liaison – Assist with application, submission, and communication with GLP certifying bodies such as NABL or CDSCO.
Contact Us for GLP Certificate Consultancy
If your organization is aiming for GLP certification to meet regulatory and international study submission requirements, contact us. Growth Management Corporation provides comprehensive GLP consultancy, training, documentation support, and audit readiness services. We help labs across pharmaceutical, chemical, biotech, and environmental sectors achieve GLP compliance and global recognition. Let us help you demonstrate scientific integrity and operational excellence with GLP.