The Log Form: Corrective and Preventive Actions (CAPA) provides a structured, GxP-compliant format for documenting the entire CAPA process — from root cause identification to final QA approval.

It ensures full traceability of all quality events, deviations, and inspection findings, supporting continuous improvement and regulatory compliance in line with ICH, EMA, and FDA expectations.
 
This form is professionally written and 99% complete, requiring only your company name and QA responsible before implementation.

It is designed for biotech and life science organizations seeking a standardized method for recording, tracking, and closing CAPAs efficiently and transparently.
 
Includes:
CAPA number and deadline tracking
Documentation of root cause and related deviation or inspection reference
Fields for corrective and preventive actions
QA approval and verification of completion
Attachment register for supporting documentation
 
This log form provides documented proof that all CAPAs are followed through to resolution, verified for effectiveness, and closed under QA oversight.
It forms a vital component of any inspection-ready QMS and demonstrates proactive quality management to regulators and partners.