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High QA offers Inspection Manager and 360 CORE for manufacturing quality planning, inspection data collection and reporting.
Verified
| Controlled document revision history | HQA 360 documents revision control and version history for drawings and inspection plans. |
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| Controlled document approval workflow | HQA 360 supports review, approval and sign-off workflows with digital traceability. |
| Electronic signatures | High QA documents digital signatures with digital traceability and multi-role workflows. |
| Training and competency records | Not documented |
| CAPA workflow | High QA links nonconformances to corrective actions. |
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| Audit management | Not documented |
| ISO 9001 focus or templates | High QA identifies ISO 9001 process and documentation requirements. |
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| Vendor-stated manufacturing positioning | Not documented |
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| Mobile quality inspections | High QA documents recording shop-floor inspection results with digital gages or tablets. |
| Nonconformance workflow | HQA 360 logs and tracks non-conformances with linked corrective actions and audit history. |
| Supplier quality | Not documented |
| Medical-device standards focus | High QA identifies ISO 13485 requirements for PPAP submission packages. |
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| 21 CFR Part 11 support statement | Not documented |
High QA offers Inspection Manager and 360 CORE for manufacturing quality planning, inspection data collection and reporting.
High QA says its PPAP submission packages align with ISO 13485 requirements. No starting price is listed in the reviewed pricing material.
