Orcanos combines medical-device eQMS workflows with ALM in a shared platform.
Orcanos names ISO 13485, EU MDR and 21 CFR Part 11 in its medical-device eQMS materials. No starting price is listed in the reviewed pricing material.
Catalog › Product profile
Orcanos combines medical-device eQMS workflows with ALM in a shared platform.
Verified
| Controlled document revision history | Not documented |
|---|---|
| Controlled document approval workflow | Not documented |
| CAPA workflow | Orcanos lists CAPA management for its eQMS. |
| Audit management | Orcanos lists audit management for its eQMS. |
| Vendor-stated manufacturing positioning | Not documented |
|---|---|
| Mobile quality inspections | Not documented |
| Nonconformance workflow | Not documented |
| Supplier quality | Orcanos lists supplier management for its eQMS. |
| Medical-device standards focus | Orcanos names ISO 13485, EU MDR and 21 CFR Part 11. |
|---|---|
| 21 CFR Part 11 support statement | Orcanos names 21 CFR Part 11 in its CAPA lifecycle compliance statement. |
| Electronic signatures | Orcanos describes e-signature in its electronic audit management offering. |
Orcanos combines medical-device eQMS workflows with ALM in a shared platform.
Orcanos names ISO 13485, EU MDR and 21 CFR Part 11 in its medical-device eQMS materials. No starting price is listed in the reviewed pricing material.