CQ Checklists and Templates
Actionable Checklists for Navigating Compliance

A three-in-one MDSAP Audit Preparation Tool kit (Part – 2)
Checklist | June, 2021
A three-in-one MDSAP Audit Preparation Tool kit (Part – 3)
Checklist | June, 2021
A three-in-one MDSAP Audit Preparation Tool kit (Part – 1)
Checklist | June, 2021
Vehicle Inspection
Checklist | June, 2021
Checklist To Prepare UDI System – EU MDR (2017/745)
Checklist | June, 2021
Checklist To Prepare UDI System – EU IVDR (2017/746)
Checklist | June, 2021
Internal Audit Tool Kit for Medical Device and IVD Manufacturer (Part – 1)
Checklist | June, 2021
Internal Audit Tool Kit for Medical Device and IVD Manufacturer (Part – 2)
Checklist | June, 2021
IVDD to IVDR – Strategic Planning & Assessment
Checklist | June, 2021
IVDR Preparedness Assessment Checklist
Checklist | June, 2021
MDR Gap Analysis & Implementation Assessment
Checklist | June, 2021
“Records” to be Maintained for an ISO 13485 Certified Device Manufacturer
Checklist | May, 2021
Post Pandemic Industry Practices For Life Science & Pharmaceuticals Manufacturing
Checklist | May, 2021
Person Responsible For Regulatory Compliance Under EU MDR & IVDR
Checklist | May, 2021
Biocompatibility Studies And Toxicological Risk Assessment Tool
Checklist | May, 2021
FDA Quality System Regulation For Labelling
Checklist | May, 2021
FDA 21 CFR Part 11 – Electronic Records Validation, Integrity And Compliance
Checklist | May, 2021
Basic Steps of Computer System Validation & Regulatory Requirements
Checklist | May, 2021
Seven Common Steps Towards Equipment or Machine Validation
Checklist | May, 2021
Remote Worker Home Office Safety Checklist
Checklist | May, 2021
Systematic Approach to Biological Evaluation with FDA’s Recommendation for Industry
Checklist | April, 2021
Eight Steps Toolkit to comply Technical Documentation for EU MDR
Checklist | April, 2021
A checklist to prepare for EUDAMED Actor Module registration
Checklist | April, 2021
Review and Update Your QMS with 50 Mandatory SOPs as per ISO 13485:2016
Checklist | April, 2021
Prepare 510(K) submission with ready-to-use checklist and advice
Checklist | April, 2021