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GLP Toolkit

GLP Toolkit

$495.00
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Downloadable Resources, Instant Access
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What does the GLP Toolkit include?

The GLP Toolkit includes 60+ downloadable files delivered via email within 24 business hours: 991 GLP assessment questions in XLSX, a pre-filled Excel dashboard with automated scoring, 49 GLP requirements in a quick-scan PDF handbook, editable SOP templates in Word, implementation workflows, maturity diagnostics, and a structured folder system including the 00_Platinum_Tier master playbook, 90-day roadmap, incident response runbook, and KPI dashboard. All content aligns with OECD Principles of Good Laboratory Practice for audit-ready compliance.

Failed GLP audits lead to rejected study data, regulatory sanctions, suspended research programmes, and irreversible damage to your laboratory’s credibility , but with the GLP Toolkit, you gain immediate access to a complete, audit-ready implementation system that ensures ongoing compliance with OECD Principles of Good Laboratory Practice. This professional development resource equips you to detect, remediate, and document full adherence to GLP standards before an inspection ever begins, eliminating costly non-conformance findings and securing the scientific validity of your non-clinical studies.

What You Receive

  • A 991-question GLP Self-Assessment in XLSX format, organised across seven OECD-compliant domains , Study Design, Test Facility Organisation, Quality Assurance, Raw Data Management, Reporting, Archiving, and Personnel Training , enabling you to identify compliance gaps in under a day
  • Pre-filled Excel Dashboard with automated scoring logic and risk heatmaps, generating regulator-ready maturity reports that highlight critical deficiencies and track remediation progress
  • 49 core GLP requirements distilled into a structured PDF Quick-Scan Handbook using the RDMAICS cycle (Recognise, Define, Measure, Analyse, Improve, Control, Sustain), so you can rapidly align internal processes with OECD GLP Principles
  • Step-by-step implementation workflows in PDF and XLSX, including role-specific checklists for Study Directors, QA Unit staff, and Lab Technicians, ensuring accountability and procedural consistency across your facility
  • Editable SOP templates in Microsoft Word format for Test Item Handling, Equipment Calibration, Deviation Management, and Data Integrity Controls , fully customisable to your organisation’s scope and audit requirements
  • Comprehensive maturity benchmarking matrices in XLSX that compare your current state against OECD GLP best practices, helping you prioritise corrective actions and demonstrate continuous improvement to regulators
  • 00_Platinum_Tier deliverables: Master GLP Implementation Playbook (PDF), 90-Day Compliance Roadmap (XLSX), GLP Incident Response Runbook (PDF), Anti-Pattern Catalogue for Audit Findings (XLSX), and KPI Observability Dashboard (XLSX)
  • Structured folder system with 60+ files: 01_Getting_Started guide, 02_Self_Assessment_and_Diagnostics, 03_Requirements_and_Goal_Setting, 04_Models_and_Frameworks, 06_Processes_and_Execution (15+ files), 07_Performance_and_KPIs, 08_Quality_and_Governance, 09_Sustainment_and_Improvement, 10_Advanced_Topics, and 11_Reference_and_Quick_Cards
  • All files delivered via email within 24 business hours as a downloadable ZIP folder , no installations, no logins, immediate offline access for your team

How This Helps You

This toolkit transforms how you manage GLP compliance: instead of reacting to audit findings, you proactively validate every aspect of your laboratory operations. With 991 targeted assessment questions, you can uncover non-conformances in hours , not weeks , and use the automated dashboard to prove compliance to internal stakeholders or regulatory bodies. The SOP templates and implementation workflows ensure consistent documentation, a requirement under OECD Guideline 17, and protect your study data from being invalidated. Without this system, laboratories risk failing inspections, losing accreditation, or having research rejected by agencies like the EPA or EMA. By implementing this framework, you future-proof your operations, reduce audit preparation time by up to 70%, and maintain scientific integrity across all non-clinical studies.

Who Is This For?

  • Study Directors responsible for ensuring test compliance with OECD GLP Principles and managing study data integrity
  • Quality Assurance Unit (QAU) Leads tasked with auditing laboratory practices and reporting to regulatory authorities
  • GLP Compliance Officers who must prepare for inspections and maintain accreditation status
  • Laboratory Managers overseeing facility operations, personnel training, and standard operating procedures
  • Regulatory Affairs Specialists supporting submissions that require GLP-certified study data
  • Pharmaceutical, agrochemical, and environmental testing lab professionals required to demonstrate adherence to OECD Guideline 17

Choosing the GLP Toolkit isn’t just an investment in documentation , it’s the strategic decision to eliminate audit risk, uphold scientific rigour, and maintain regulatory trust. For professionals responsible for non-clinical study validity, this is the definitive system to implement, sustain, and prove full compliance with OECD GLP standards.

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