Procedures for Addressing Weight Variation Issues

1) Purpose

The purpose of this SOP is to outline the actions to be taken when the weight variation of filled capsules exceeds acceptable limits, including documentation and investigation procedures.

2) Scope

This SOP applies to all filled capsules produced within the pharmaceutical manufacturing facility that are found to have weight variation exceeding acceptable limits.

3) Responsibilities

The Quality Control (QC) department is responsible for identifying weight variation issues and implementing corrective actions. The Production department is responsible for addressing and documenting these issues.

4) Procedure

1. Identification of Weight Variation Issues:
   1. During routine weight checks, identify any capsules that fall outside the acceptable weight variation limits.
   2. Document the non-conforming weights in the weight variation logbook.
2. Immediate Actions:
   1. Isolate the affected batch or lot of capsules to prevent further processing or distribution.
   2. Notify the QC manager and relevant personnel about the weight variation issue.
3. Investigation:
   1. Conduct a thorough investigation to determine the root cause of the weight variation issue.
   2. Review the manufacturing process, equipment calibration records, and operator logs for potential causes.
   3. Document the findings of the investigation in a deviation report.
4. Corrective and Preventive Actions (CAPA):
   1. Develop and implement corrective actions to address the identified root cause.
   2. Implement preventive