F-QM-013-A-V0 — Management Review Record & Action Follow-Up Log
Type: Form · Version: V0 · Status: DRAFT — UNAPPROVED · Served read-only from the bundled QMS copies. The Drive master is untouched.
Parent document: LAB-QM-013 — Management Review Policy (parent is encoded in the form number)
Rendered in-browser from the project's Word file F-QM-013-A-V0-management-review-record.docx (policies-docx / forms-docx — the file Junry reviews). Formatting is faithful, not pixel-perfect; the DOCX is the official copy.
| Document # | F-QM-013-A-V0 | Parent Document | LAB-QM-013 — Management Review Policy |
|---|
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# SECTION A — ANNUAL MANAGEMENT REVIEW RECORD
Part 1 — Review Identification & Meeting Type
| Field | Details |
|---|---|
| Review Reference No.: | MR-YYYY-____ |
| Date(s) Conducted: | YYYY-MM-DD |
| Meeting Venue: | Hospital Conference Room / Administrative Office |
| Review Type: | [ ] Annual Scheduled Review [ ] Extraordinary Review (Trigger: ________________________) |
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Part 2 — Participants & Quorum
| Governance Role | Name | Present | Signature |
|---|---|---|---|
| Hospital Director (Chair): | [ ] Yes [ ] No | ||
| Pathologist / Head of Laboratory: | [ ] Yes [ ] No | ||
| Chief Medical Technologist / LQM (Secretary): | Junry, RMT | [ ] Yes [ ] No | |
| Safety Officer / Invited Personnel: | [ ] Yes [ ] No |
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Part 3 — Planned Input Agenda & Evaluation Summary
Review of the required quality management inputs per LAB-QM-013 Section 5.4:
| # | Mandatory Input Agenda Area | Sourced Record Reference | Summary of Deliberations & Findings |
|---|---|---|---|
| 1 | Status of actions from previous reviews | F-QM-013-A Section B | All previous action items reviewed; carryover noted below. |
| 2 | Internal and external changes affecting QMS | Hospital / DOH updates | Scope, staffing, and regulatory inspection updates reviewed. |
| 3 | Workload volume and clinical services | LIS test statistics | Primary test volume trends and referral patterns evaluated. |
| 4 | Adequacy of physical and human resources | Budget / Staffing review | Analyzer reagents, staffing complement, and UPS capacity reviewed. |
| 5 | Fulfilment of annual quality objectives | F-QM-001-A Part 4 | Progress on strategic quality goals and annual targets evaluated. |
| 6 | Internal audit findings & nonconformities | F-QM-012-A / F-QM-010-A | Cycle 1 and Cycle 2 audit findings and root causes reviewed. |
| 7 | External regulatory and PT assessments | NEQAS / DOH LTO records | Proficiency testing performance and DOH licensing checklist audited. |
| 8 | Quality indicators performance trends | F-QM-003-A Part 1 & 2 | Turnaround time, specimen rejection, and critical value metrics. |
| 9 | Status of corrective & preventive actions | F-QM-011-A Section B | Closed-loop effectiveness of open and completed CAPAs. |
| 10 | Client feedback, complaints, and surveys | F-QM-004-A Section B & D | Patient satisfaction scores (>=90% target) and complaint resolution. |
| 11 | Continuous quality improvement studies | F-QM-003-B Section A | Ongoing PDCA charters and clinical study outcomes evaluated. |
| 12 | Recommendations for system improvement | Staff submissions | New opportunities for workflow digitization and bench enhancements. |
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Part 4 — Management Review Decisions & System Outputs
| Output Dimension | Executive Decisions & Directives Approved by Hospital Director & Pathologist |
|---|---|
| 1. QMS Effectiveness & Policies: | Approval of updated Quality Management Manual, policies, and continuous compliance measures. |
| 2. Clinical Service Improvements: | Specific measures to streamline outpatient turnaround time and specimen collection quality. |
| 3. Resource Allocations: | Budgetary commitments for analyzer service contracts, backup power maintenance, and staff CPD. |
| 4. Quality Objectives for Next Year: | Approved revisions to Key Performance Indicators and new annual targets. |
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# SECTION B — MANAGEMENT REVIEW ACTION & FOLLOW-UP LOG
The Chief Medical Technologist / Laboratory Quality Manager maintains this log to track all management directives through completion:
| Action Ref No. | Source MR Ref / Date | Action / Decision Description | Routing (CAPA / Risk / CQI / Admin) | Responsible Owner | Required Resources | Target Due Date | Status | Completion Date | Verification Notes | Carryover to Next MR? |
|---|---|---|---|---|---|---|---|---|---|---|
| MR-ACT-01 | [ ] Open [ ] Closed | [ ] Yes [ ] No | ||||||||
| MR-ACT-02 | [ ] Open [ ] Closed | [ ] Yes [ ] No | ||||||||
| MR-ACT-03 | [ ] Open [ ] Closed | [ ] Yes [ ] No | ||||||||
| MR-ACT-04 | [ ] Open [ ] Closed | [ ] Yes [ ] No |
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Part 5 — Executive Concurrence & Authorization
| Role | Name | Signature | Date |
|---|---|---|---|
| Documented by: Chief Medical Technologist / LQM | Junry, RMT | ||
| Reviewed by: Pathologist / Head of Laboratory | |||
| Approved by: Hospital Director |
