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Corrective and Preventive Action (CAPA) Form

Form ID FRM-003 Revision 1.0

Section 1: CAPA Identification

Field Entry
CAPA Number
Date Initiated
Initiated By
CAPA Owner
Target Closure Date

Section 2: Classification

Type

  • Corrective Action
  • Preventive Action

Source

  • Patient Safety Event
  • Medication Error
  • Healthcare-Associated Infection
  • Equipment Failure
  • Internal Audit
  • External Audit/Survey
  • Family Complaint
  • Process Deviation
  • Sentinel Event
  • Management Review
  • Other: ____________

Priority

  • Critical (patient harm occurred or high risk - 5 business days)
  • Major (potential for patient harm - 15 business days)
  • Minor (process deviation, no patient impact - 30 business days)

Section 3: Problem Description

(Describe the nonconformity or potential nonconformity - include patient impact if applicable)

Section 4: Immediate Containment

(Actions taken to contain the immediate impact and protect patient safety)

Section 5: Root Cause Investigation

Investigation Method Used

  • Root Cause Analysis (RCA)
  • Failure Mode and Effects Analysis (FMEA)
  • 5 Whys
  • Fishbone Diagram
  • Fault Tree Analysis
  • Other: ____________

Root Cause Determination

Contributing Factors

Section 6: Corrective/Preventive Actions

Action Responsible Due Date Status

Section 7: Staff Communication and Training

Training/Communication Required Target Audience Completion Date

Section 8: Effectiveness Verification

Criteria Method Result

Verification Date: ____________ Verified By: ____________

Section 9: Closure

Role Name Signature Date
CAPA Owner
Quality Approval

Lessons Learned


Form FRM-003 Rev 1.0