{"product_id":"ims-non-clinical-r-and-d-laboratories-glp-iso-iec-17025-iso-15189-iso-9001","title":"IMS Non-Clinical R\u0026D Laboratories (GLP, ISO\/IEC 17025, ISO 15189, ISO 9001)","description":"\u003cp\u003eThis comprehensive Integrated Management System — the most extensive in the catalog — serves non-clinical research and development laboratories conducting safety and regulatory studies. It integrates OECD GLP Principles, FDA 21 CFR Part 58, ISO\/IEC 17025, ISO 15189, and ISO 9001 into a single, rigorously controlled framework built for regulatory study integrity. The documentation governs the complete GLP study lifecycle: study plans and protocols, Study Director and personnel responsibilities, test-item characterization and handling, standard operating procedures, raw-data capture, archiving, and final report certification. A dedicated Quality Assurance program, independent of study conduct, provides the inspections and audits GLP demands. A master Quality Manual and compliance scheme map every principle to a control, while an exceptionally deep procedure and form library enforces traceable, reconstructable data and full chain-of-custody. Checklists mirror regulatory inspection modules, and training modules build and document the competencies of Study Directors, technicians, and QA staff. The ISO\/IEC 17025 and 15189 layers add technical-competence rigor for analytical and bioanalytical work. This kit is ideal for CROs, toxicology and bioanalytical labs, and R\u0026amp;D facilities preparing for GLP monitoring-authority inspection or study-sponsor audits. Fully editable, it adapts to your study types, test systems, and facilities. By systematizing study conduct, data integrity, and independent QA, it protects study validity, withstands regulatory scrutiny, and accelerates the acceptance of your data in submissions — turning GLP compliance into a durable competitive and scientific advantage.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eIncluded:\u003c\/strong\u003e 88 ready-to-use, fully editable documents (manual, procedures, forms, records, checklists, guidance and training material).\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eLicense:\u003c\/strong\u003e single-organization license; delivered electronically as a ZIP archive.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56517064393044,"sku":"AGS-07-015","price":3800.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/IMS-Non-Clinical-R-D-Laboratories-GLP-ISO-IEC-17025-ISO-15189-ISO-9001.png?v=1784574573","url":"https:\/\/agskits.com\/products\/ims-non-clinical-r-and-d-laboratories-glp-iso-iec-17025-iso-15189-iso-9001","provider":"apex global solutions","version":"1.0","type":"link"}