ISO 13485 Medical Device QMS Starter
Quality manual, 10 core procedures, DHF/DMR/DHR templates, ISO 14971-style risk file, CAPA and complaint logs.
What's inside →Quality system, risk, design controls, validation, complaints, cleanroom and EU MDR templates for small medical device makers and contract manufacturers. All files are templates, not regulatory advice or certification.
18 kits · instant download · editable Word & Excel
Quality manual, 10 core procedures, DHF/DMR/DHR templates, ISO 14971-style risk file, CAPA and complaint logs.
What's inside →Gap assessment mapping the old QSR to the QMSR / ISO 13485, a records matrix and a transition plan. Templates, not regulatory advice.
What's inside →Risk plan, hazard analysis tied to an editable acceptability matrix, FMEA, benefit-risk and the risk management report. Templates, not regulatory advice.
What's inside →Traceability matrix with gap flags, design plan, design review, V&V protocol/report and design transfer templates. Templates, not regulatory advice.
What's inside →Master validation plan, IQ/OQ/PQ protocols and reports, and a sample-size and Ppk calculator. Templates, not regulatory advice.
What's inside →Intake and investigation forms, 21 CFR 803 reportability decision tree, complaint log with due dates and trending. Templates, not regulatory advice.
What's inside →Monitoring log with alert/action flags, gowning qualification, cleaning record and excursion form. Templates, not regulatory advice.
What's inside →Technical documentation index, GSPR checklist structure, PMS data log, PMS plan and PSUR templates. Templates, not regulatory advice.
What's inside →Endpoint matrix with gap flags, device categorization, materials inventory, biological evaluation plan and report shell. Templates, not regulatory advice.
What's inside →Validation tracker for EO, steam and radiation, requalification calendar, BI and dose release log, protocol and report. Templates, not regulatory advice.
What's inside →Lifecycle checklist, requirements-to-test traceability, SOUP register, problem reports, SDP and release checklist. Templates, not regulatory advice.
What's inside →Use specification, use-related risk analysis with critical-task flags, formative/summative test log and HFE summary. Templates, not regulatory advice.
What's inside →Risk-based approved supplier list with audit-due flags, scorecard, SCAR log, quality agreement and procedure. Templates, not regulatory advice.
What's inside →Readiness tracker for the 7 MDSAP audit processes, 5-jurisdiction checklist, NC grading worksheet and audit plan. Templates, not regulatory advice.
What's inside →UDI-DI register with GUDID/EUDAMED flags, US and EU label review checklist, label change form and procedure. Templates, not regulatory advice.
What's inside →Threat model, exploitability-based risk assessment, SBOM inventory, vulnerability log and submission checklist. Not regulatory advice.
What's inside →Packaging gap tracker by ISO 11607-1/-2 clause, seal-strength workbook with Ppk, accelerated-aging calculator, validation master plan, sealer IQ/OQ/PQ protocol and distribution/aging test plan. Templates, not regulatory advice.
What's inside →Not eligible for NQT documentation review (all kits in this bundle). 15 medical device quality kits in one download of editable Word and Excel templates for small device makers and contract manufacturers. $975 if bought separately: save $678.
What's inside →Every medical kit, new medical templates each month, a plain-English regulatory watch note (FDA QMSR, EU MDR) and a monthly live Q&A. Planned at $29/month or $249/year. Templates and education, not regulatory advice. Grab the free checklist to hear when it opens.