# Conduct Gxp Audit

> Conduct a GxP audit of computerized systems and processes. Covers audit planning, opening meetings, evidence collection, finding classification (critical/major/minor), CAPA generation, closing meetings, report writing, and follow-up verification. Use for scheduled internal audits, supplier qualification audits, pre-inspection readiness assessments, for-cause audits triggered by deviations or data integrity concerns, or periodic compliance posture reviews of validated systems.

- Skill: `pjt222/conduct-gxp-audit-6` (Agent Skill)
- Install (CLI): `npx skillmds@latest add pjt222/conduct-gxp-audit-6`
- Raw SKILL.md: https://api.skillmd.com/api/skills/pjt222/conduct-gxp-audit-6/raw
- Safety review: pending (external: skill-scanner PASS, skillspector PASS)
- Works with: Claude Code, Claude.ai, OpenAI Codex
- Category: Security
- License: MIT
- Author: pjt222 (https://skillmd.com/u/pjt222)
- Updated: 2026-09-21
- Page: https://skillmd.com/skills/pjt222/conduct-gxp-audit-6

---


# Conduct GxP Audit

Plan and execute GxP audit of computerized systems, data integrity practices, or regulated processes.

## When Use

- Scheduled internal audit of validated computerized system
- Supplier/vendor qualification audit for GxP-relevant software
- Pre-inspection readiness assessment before regulatory audit
- For-cause audit triggered by deviation, complaint, or data integrity concern
- Periodic review of validated system compliance posture

## Inputs

- **Required**: Audit scope (system, process, or site to audit)
- **Required**: Applicable regulations (21 CFR Part 11, EU Annex 11, GMP, GLP, GCP)
- **Required**: Previous audit reports, open CAPA items
- **Optional**: System validation documentation (URS, VP, IQ/OQ/PQ, traceability matrix)
- **Optional**: SOPs, training records, change control logs
- **Optional**: Specific risk areas or concerns triggering audit

## Steps

### Step 1: Develop Audit Plan

```markdown
# Audit Plan
## Document ID: AP-[SYS]-[YYYY]-[NNN]

### 1. Objective
[State the purpose: scheduled, for-cause, supplier qualification, pre-inspection]

### 2. Scope
- **System/Process**: [Name and version]
- **Regulations**: [21 CFR Part 11, EU Annex 11, ICH Q7, etc.]
- **Period**: [Date range of records under review]
- **Exclusions**: [Any areas explicitly out of scope]

### 3. Audit Criteria
| Area | Regulatory Reference | Key Requirements |
|------|---------------------|------------------|
| Electronic records | 21 CFR 11.10 | Controls for closed systems |
| Audit trail | 21 CFR 11.10(e) | Secure, computer-generated, time-stamped |
| Electronic signatures | 21 CFR 11.50 | Manifestation, legally binding |
| Access controls | EU Annex 11, §12 | Role-based, documented |
| Data integrity | MHRA guidance | ALCOA+ principles |
| Change control | ICH Q10 | Documented, assessed, approved |

### 4. Schedule
| Date | Time | Activity | Participants |
|------|------|----------|-------------|
| Day 1 AM | 09:00 | Opening meeting | All |
| Day 1 AM | 10:00 | Document review | Auditor + QA |
| Day 1 PM | 13:00 | System walkthrough | Auditor + IT + System Owner |
| Day 2 AM | 09:00 | Interviews + evidence collection | Auditor + Users |
| Day 2 PM | 14:00 | Finding consolidation | Auditor |
| Day 2 PM | 16:00 | Closing meeting | All |

### 5. Audit Team
| Role | Name | Responsibility |
|------|------|---------------|
| Lead Auditor | [Name] | Plan, execute, report |
| Subject Matter Expert | [Name] | Technical assessment |
| Auditee Representative | [Name] | Facilitate access and information |
```

**Got:** Audit plan approved by quality management, communicated to auditee at least 2 weeks before audit.
**If fail:** Reschedule if auditee cannot provide required documentation or personnel.

### Step 2: Conduct Opening Meeting

Agenda:
1. Introduce audit team, roles
2. Confirm scope, schedule, logistics
3. Explain finding classification system (critical/major/minor)
4. Confirm confidentiality agreements
5. Identify auditee escorts, document custodians
6. Address questions

**Got:** Opening meeting documented with attendance record.
**If fail:** Key personnel unavailable? Reschedule affected audit activities.

### Step 3: Collect and Review Evidence

Review documentation, records against audit criteria:

#### 3a. Validation Documentation Review
- [ ] URS exists, approved
- [ ] Validation plan matches system category, risk
- [ ] IQ/OQ/PQ protocols executed with results documented
- [ ] Traceability matrix links requirements to test results
- [ ] Deviations documented, resolved
- [ ] Validation summary report approved

#### 3b. Operational Controls Review
- [ ] SOPs current, approved
- [ ] Training records demonstrate competence for all users
- [ ] Change control records complete (request, assessment, approval, verification)
- [ ] Incident/deviation reports handled per SOP
- [ ] Periodic review conducted on schedule

#### 3c. Data Integrity Assessment
- [ ] Audit trail enabled, not modifiable by users
- [ ] Electronic signatures meet regulatory requirements
- [ ] Backup and recovery procedures documented, tested
- [ ] Access controls enforce role-based permissions
- [ ] Data is attributable, legible, contemporaneous, original, accurate (ALCOA+)

#### 3d. System Configuration Review
- [ ] Production configuration matches validated state
- [ ] User accounts reviewed — no shared accounts, inactive accounts disabled
- [ ] System clocks synchronized, accurate
- [ ] Security patches applied per approved change control

**Got:** Evidence collected as screenshots, document copies, interview notes with timestamps.
**If fail:** Record "unable to verify" as observation, note reason.

### Step 4: Classify Findings

Classify each finding by severity:

| Classification | Definition | Response Required |
|---|---|---|
| **Critical** | Direct impact on product quality, patient safety, or data integrity. Systematic failure of a key control. | Immediate containment + CAPA within 15 business days |
| **Major** | Significant departure from GxP requirements. Potential to impact data integrity if uncorrected. | CAPA within 30 business days |
| **Minor** | Isolated deviation from procedure. No direct impact on data integrity or product quality. | Correction within 60 business days |
| **Observation** | Opportunity for improvement. Not a regulatory requirement. | Optional — tracked for trend analysis |

Document each finding:

```markdown
## Finding F-[NNN]
**Classification:** [Critical / Major / Minor / Observation]
**Area:** [Audit trail / Access control / Change control / etc.]
**Reference:** [Regulatory clause, e.g., 21 CFR 11.10(e)]

**Observation:**
[Objective description of what was found]

**Evidence:**
[Document ID, screenshot reference, interview notes]

**Regulatory Expectation:**
[What the regulation requires]

**Risk:**
[Impact on data integrity, product quality, or patient safety]
```

**Got:** Every finding has classification, evidence, regulatory reference.
**If fail:** Classification disputed? Escalate to audit program manager for adjudication.

### Step 5: Conduct Closing Meeting

Agenda:
1. Present findings summary (no new findings should be raised)
2. Review finding classifications
3. Discuss preliminary CAPA expectations, timelines
4. Confirm next steps, report timeline
5. Acknowledge auditee cooperation

**Got:** Closing meeting documented with attendance. Auditee acknowledges findings (acknowledgement ≠ agreement).
**If fail:** Auditee disputes finding? Document disagreement, escalate per SOP.

### Step 6: Write Audit Report

```markdown
# Audit Report
## Document ID: AR-[SYS]-[YYYY]-[NNN]

### 1. Executive Summary
An audit of [System/Process] was conducted on [dates] against [regulations].
[N] findings were identified: [n] critical, [n] major, [n] minor, [n] observations.

### 2. Scope and Methodology
[Summarize audit plan scope, criteria, and methods used]

### 3. Findings Summary
| Finding ID | Classification | Area | Brief Description |
|-----------|---------------|------|-------------------|
| F-001 | Major | Audit trail | Audit trail disabled for batch record module |
| F-002 | Minor | Training | Two users missing annual GxP training |
| F-003 | Observation | Documentation | SOP formatting inconsistencies |

### 4. Detailed Findings
[Include full finding details from Step 4 for each finding]

### 5. Positive Observations
[Document areas of good practice observed during the audit]

### 6. Conclusion
The overall compliance status is assessed as [Satisfactory / Needs Improvement / Unsatisfactory].

### 7. Distribution
| Recipient | Role |
|-----------|------|
| [Name] | System Owner |
| [Name] | QA Director |
| [Name] | IT Manager |

### Approval
| Role | Name | Signature | Date |
|------|------|-----------|------|
| Lead Auditor | | | |
| QA Director | | | |
```

**Got:** Report issued within 15 business days of closing meeting.
**If fail:** Delayed beyond 15 days? Notify stakeholders, document reason.

### Step 7: Track CAPA and Verify Effectiveness

For each finding requiring CAPA:

```markdown
## CAPA Tracking
| Finding ID | CAPA ID | Root Cause | Corrective Action | Due Date | Status | Effectiveness Check |
|-----------|---------|------------|-------------------|----------|--------|-------------------|
| F-001 | CAPA-2025-042 | Configuration oversight during upgrade | Enable audit trail, verify all modules | 2025-04-15 | Open | Scheduled 2025-07-15 |
| F-002 | CAPA-2025-043 | Training matrix not updated | Complete training, update tracking | 2025-05-01 | Open | Scheduled 2025-08-01 |
```

**Got:** CAPAs assigned, tracked, effectiveness verified per defined timeline.
**If fail:** Unresolved CAPAs escalate to QA management, flagged in next audit cycle.

## Checks

- [ ] Audit plan approved, communicated before audit
- [ ] Opening and closing meetings documented with attendance
- [ ] Evidence collected with timestamps, source references
- [ ] Every finding has classification, evidence, regulatory reference
- [ ] Audit report issued within 15 business days
- [ ] CAPAs assigned with due dates for all critical and major findings
- [ ] Previous audit CAPAs verified for closure effectiveness

## Pitfalls

- **Scope creep**: Expanding audit scope during execution without formal agreement leads to incomplete coverage, disputes.
- **Opinion-based findings**: Findings must reference specific regulatory requirements, not personal preferences.
- **Adversarial tone**: Audits are collaborative quality improvement exercises, not interrogations.
- **Ignoring positives**: Reporting only findings without acknowledging good practices undermines trust.
- **No effectiveness check**: Closing CAPA without verifying fix actually works is recurring regulatory citation.

## See Also

- `perform-csv-assessment` — full CSV lifecycle assessment (URS through validation summary)
- `setup-gxp-r-project` — project structure for validated R environments
- `implement-audit-trail` — audit trail implementation for electronic records
- `write-validation-documentation` — IQ/OQ/PQ protocol, report writing
- `security-audit-codebase` — security-focused code audit (complementary perspective)