Controlled Documents (testcompany1)
Manage compliance records and document lifecycles.
Filter by Status
| ID / Number | Document Title | Version | Status | Last Modified | |
|---|---|---|---|---|---|
DHF-001 | Design History File: Surgical Forceps SF-200 | 4.0 | EFFECTIVE | 3/10/2026 | |
RA-002 | Risk Assessment: Scalpel Handle SH-100 | 1.1 | UNDER_REVIEW | 3/10/2026 | |
RA-001 | Risk Assessment: Surgical Forceps SF-200 | 2.0 | EFFECTIVE | 3/10/2026 | |
FORM-003 | Change Request Intake Form | 1.0 | DRAFT | 3/10/2026 | |
FORM-002 | Design Review Record Template | 2.0 | EFFECTIVE | 3/10/2026 | |
FORM-001 | Nonconformance Report Template | 1.0 | EFFECTIVE | 3/10/2026 | |
WI-003 | Packaging & Labeling Instruction | 2.2 | UNDER_REVIEW | 3/10/2026 | |
WI-002 | Final Inspection Checklist | 3.1 | EFFECTIVE | 3/10/2026 | |
WI-001 | Sterilization Process Work Instruction | 5.0 | EFFECTIVE | 3/10/2026 | |
SOP-008 | Validation & Verification Procedure | 2.0 | APPROVED | 3/10/2026 | |
SOP-007 | Management Review Procedure | 1.1 | EFFECTIVE | 3/10/2026 | |
SOP-006 | Internal Audit Procedure | 1.0 | DRAFT | 3/10/2026 | |
SOP-005 | Risk Management Procedure (ISO 14971) | 3.2 | EFFECTIVE | 3/10/2026 | |
SOP-004 | CAPA Management Procedure | 2.0 | EFFECTIVE | 3/10/2026 | |
SOP-003 | Supplier Qualification Procedure | 1.3 | UNDER_REVIEW | 3/10/2026 | |
SOP-002 | Design & Development Procedure | 4.0 | EFFECTIVE | 3/10/2026 | |
SOP-001 | Document Control Procedure | 2.1 | EFFECTIVE | 3/10/2026 | |
SOP-101 | Manufacturing SOP - Test Company One (Medical Devices) | 1.0 | UNDER_REVIEW | 3/10/2026 | |
QM-001 | Quality Manual - Test Company One (Medical Devices) | 1.0 | APPROVED | 3/10/2026 |