CQ Checklists and Templates
Actionable Checklists for Navigating Compliance
Join ConQuest 2025 | ComplianceQuest User Conference | April 8–10, Clearwater Beach, FL
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Pharmaceutical CGMP Regulations with Quality System Part 1
Checklist | July, 2021
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Check the Completeness of Your EU Declaration of Conformity
Checklist | July, 2021
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Ladder Inspection
Checklist | July, 2021
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Health and Safety Assessment Checklist for the General Office Building
Checklist | July, 2021
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Five Steps Corrective and Prevention Action (CAPA) Reporting Template
Checklist | July, 2021
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MDSAP Remote Audit
Checklist | July, 2021
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EHS RFP Template
Checklist | July, 2021
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A Three-in-One MDSAP Audit Preparation Tool kit (Part – 2)
Checklist | June, 2021
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A Three-in-One MDSAP Audit Preparation Tool kit (Part – 3)
Checklist | June, 2021
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A Three-in-One MDSAP Audit Preparation Tool kit (Part – 1)
Checklist | June, 2021
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Vehicle Inspection
Checklist | June, 2021
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Checklist To Prepare UDI System – EU MDR (2017/745)
Checklist | June, 2021
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Checklist To Prepare UDI System – EU IVDR (2017/746)
Checklist | June, 2021
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Internal Audit Tool Kit for Medical Device and IVD Manufacturer (Part – 1)
Checklist | June, 2021
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Internal Audit Tool Kit for Medical Device and IVD Manufacturer (Part – 2)
Checklist | June, 2021
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IVDD to IVDR – Strategic Planning & Assessment
Checklist | June, 2021
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IVDR Preparedness Assessment Checklist
Checklist | June, 2021
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MDR Gap Analysis & Implementation Assessment
Checklist | June, 2021
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“Records” to be Maintained for an ISO 13485 Certified Device Manufacturer
Checklist | May, 2021
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Post Pandemic Industry Practices For Life Science & Pharmaceuticals Manufacturing
Checklist | May, 2021
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Person Responsible For Regulatory Compliance Under EU MDR & IVDR
Checklist | May, 2021
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Biocompatibility Studies And Toxicological Risk Assessment Tool
Checklist | May, 2021
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FDA Quality System Regulation For Labelling
Checklist | May, 2021
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FDA 21 CFR Part 11 – Electronic Records Validation, Integrity And Compliance
Checklist | May, 2021
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Basic Steps of Computer System Validation & Regulatory Requirements
Checklist | May, 2021
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Seven Common Steps Towards Equipment or Machine Validation
Checklist | May, 2021
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Remote Worker Home Office Safety Checklist
Checklist | May, 2021
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Systematic Approach to Biological Evaluation with FDA’s Recommendation for Industry
Checklist | April, 2021
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Eight Steps Toolkit to comply Technical Documentation for EU MDR
Checklist | April, 2021
