191 lines
5.0 KiB
Markdown
191 lines
5.0 KiB
Markdown
# Standard Operating Procedure: Corrective and Preventive Action (CAPA)
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| Document ID | SOP-002 |
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| Title | Corrective and Preventive Action (CAPA) |
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| Revision | 1.0 |
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| Effective Date | [DATE] |
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| Author | [AUTHOR] |
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| Approved By | [APPROVER] |
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| Department | Quality Assurance |
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---
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## 1. Purpose
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To establish a systematic approach for identifying, investigating, and addressing nonconformities, clinical errors, and opportunities for improvement in developmental pediatric services.
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## 2. Scope
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This procedure applies to all aspects of developmental pediatric services including:
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- Diagnostic assessment procedures
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- Screening programs
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- School liaison activities
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- Clinical operations
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- Documentation and reporting
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- Family communication
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- Multidisciplinary coordination
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- Safety incidents
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## 3. Responsibilities
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### 3.1 All Staff
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- Report nonconformities, incidents, and improvement opportunities
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- Participate in CAPA investigations
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- Implement assigned corrective actions
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### 3.2 Quality Assurance Manager
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- Coordinates CAPA process
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- Assigns CAPA owners
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- Tracks CAPA completion
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- Reports CAPA metrics to management
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### 3.3 CAPA Owner
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- Investigates root cause
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- Develops action plan
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- Implements corrective/preventive actions
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- Verifies effectiveness
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### 3.4 Clinical Director
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- Reviews clinical CAPAs
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- Approves clinical protocol changes
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- Ensures assessment standardization maintained
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## 4. Definitions
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| Term | Definition |
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|------|------------|
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| Nonconformity | Failure to meet specified requirements or standards |
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| Corrective Action | Action to eliminate the cause of a detected nonconformity |
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| Preventive Action | Action to eliminate the cause of a potential nonconformity |
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| Root Cause | Fundamental reason for occurrence of a problem |
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## 5. Procedure
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### 5.1 CAPA Initiation
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CAPAs may be initiated from:
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- Internal audits
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- Management reviews
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- Clinical incident reports
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- Family complaints
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- Assessment protocol deviations
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- Documentation errors
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- Diagnostic discrepancies
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- School liaison communication issues
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- Training gaps
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- Equipment/tool malfunctions
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### 5.2 CAPA Documentation
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1. Complete FRM-003 CAPA Form
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2. Describe the issue in detail
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3. Include relevant data (dates, affected cases, assessment tools involved)
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4. Assign severity level:
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- **Critical**: Affects patient safety or diagnostic accuracy
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- **Major**: Significant impact on service quality
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- **Minor**: Limited impact, easily corrected
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### 5.3 Root Cause Analysis
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1. CAPA Owner assigned by QA Manager
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2. Gather facts and data
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3. Use appropriate analysis tools:
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- 5 Whys
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- Fishbone diagram
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- Timeline analysis
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4. Consider contributing factors:
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- Training adequacy
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- Protocol clarity
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- Assessment tool fidelity
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- Communication breakdown
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- Workload/scheduling
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- Documentation systems
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5. Document root cause findings
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### 5.4 Action Plan Development
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1. Identify corrective actions to address root cause
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2. Identify preventive actions to prevent recurrence
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3. Assign responsibilities and target completion dates
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4. Consider impact on:
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- Assessment standardization
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- Clinical protocols
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- Staff training
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- Documentation systems
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- Related processes
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### 5.5 Implementation
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1. Execute action plan
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2. Document implementation activities
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3. Update affected procedures/protocols
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4. Provide staff training if needed
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5. Communicate changes to relevant personnel
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### 5.6 Effectiveness Check
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1. Verify actions implemented as planned
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2. Monitor for recurrence (minimum 30 days)
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3. Review relevant metrics:
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- Assessment completion rates
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- Documentation accuracy
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- Family satisfaction
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- Protocol adherence
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4. Document effectiveness check results
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### 5.7 CAPA Closure
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1. QA Manager reviews for completeness
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2. Verify all actions completed
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3. Confirm effectiveness demonstrated
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4. Close CAPA in tracking system
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5. Archive CAPA records
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### 5.8 Trending and Analysis
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1. QA reviews CAPA data quarterly
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2. Identify trends and patterns
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3. Report findings to management
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4. Initiate preventive actions for recurring issues
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## 6. Special Considerations for Clinical CAPAs
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### 6.1 Assessment Protocol Deviations
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- Document impact on diagnostic validity
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- Review with Clinical Director
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- Consider need for case re-evaluation
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- Update assessment training
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### 6.2 Diagnostic Discrepancies
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- Review assessment data and scoring
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- Verify DSM-5-TR criteria application
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- Consider multidisciplinary team review
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- Document clinical reasoning
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### 6.3 School Liaison Issues
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- Review IEP/504 documentation accuracy
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- Verify IDEA compliance
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- Improve school communication protocols
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## 7. Related Documents
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- FRM-003 CAPA Form
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- SOP-001 Document Control
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- SOP-004 Internal Audit
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- Clinical Incident Report Form
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## 8. References
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- ISO 9001:2015 Clause 10.2 (Nonconformity and Corrective Action)
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- Clinical quality improvement methodologies
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- Patient safety best practices
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---
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## Revision History
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| Rev | Date | Description | Author |
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|-----|------|-------------|--------|
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| 1.0 | [DATE] | Initial release | [AUTHOR] |
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