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Propel QMS is a standalone quality management system with document control, remediation, supplier quality and audit workflows.
Verified
| Controlled document revision history | Propel QMS manages document revisions and retains change history. |
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| Controlled document approval workflow | Propel QMS documents include approval workflows. |
| Electronic signatures | Propel describes electronic records and signatures for its MedTech compliance offering. |
| Training and competency records | Propel QMS manages employee certification and document-based training programs. |
| CAPA workflow | Propel QMS describes CAPA processes for investigation and remedial action. |
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| Audit management | Propel QMS supports audit processes from planning to reporting. |
| ISO 9001 focus or templates | Propel names ISO 9001:2015 requirements. |
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| Vendor-stated manufacturing positioning | Not documented |
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| Mobile quality inspections | Not documented |
| Nonconformance workflow | Propel QMS records non-conforming materials and supports disposition and resolution workflows. |
| Supplier quality | Propel QMS includes supplier qualification and supplier corrective action workflows. |
| Medical-device standards focus | Propel names ISO 13485:2016, EU MDR and FDA 21 CFR Part 820. |
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| 21 CFR Part 11 support statement | Propel describes its offering as supporting FDA 21 CFR Part 11 requirements. |
Propel QMS is a standalone quality management system with document control, remediation, supplier quality and audit workflows.
Propel names ISO 13485:2016, EU MDR and FDA 21 CFR Part 820 for medical-device quality. No starting price is listed in the reviewed pricing material.
