manufacturing areas are monitored consistently. The QC Manager ensures that humidity monitoring devices are calibrated and functioning as expected. The QA Manager ensures that the process is compliant with this SOP.

5. Procedure

5.1 Preparation for Humidity Monitoring

1. Ensure that all humidity monitoring devices, such as hygrometers or humidity sensors, are calibrated and functioning correctly.
2. Confirm that the manufacturing areas are properly set up for tablet production, including appropriate airflow, temperature, and humidity control systems.
3. Verify that the environmental conditions (temperature and humidity) are within the acceptable limits specified in the batch record or product specifications.

5.2 Monitoring Humidity Levels

1. Monitor the humidity levels at regular intervals during tablet manufacturing, particularly during critical steps such as blending, granulation, and drying.
2. Record the humidity levels at specified intervals (e.g., every 2 hours) in the batch record (Annexure-2), including the time, date, and location of the reading.
3. Ensure that humidity levels remain within the specified range, typically between 40% and 60% relative humidity (RH) for most tablet manufacturing processes.
4. If automated humidity monitoring systems are in place, verify that the systems are functioning properly and that data logs are being captured automatically.

5.3 Adjusting Humidity Levels

1. If humidity levels are found to be outside the specified range, take immediate corrective action. Adjust the air conditioning, dehumidifiers, or humidifiers as necessary to bring the humidity levels back within the acceptable limits.
2. If manual adjustments are required, verify the settings and functionality of the HVAC systems and environmental controls in the manufacturing area.
3. Notify the QC and QA teams about the deviation and ensure that corrective actions are documented in the deviation report (Annexure-1).

5.4 Documentation of Humidity Levels

1. Document all humidity readings in the batch record (Annexure-2), including any corrective actions taken to address deviations in humidity levels.
2. Ensure that the recorded humidity levels are reviewed periodically by the QA team for compliance with product specifications.
3. Keep records of humidity monitoring for the required retention period, as specified in the company’s document retention policy.

5.5 Corrective Actions for Humidity Deviations

1. If humidity levels exceed the specified range for a prolonged period, investigate the root cause. Potential causes may include malfunctioning HVAC systems, insufficient ventilation, or improper room setup.
2. Adjust the manufacturing environment, equipment settings, or process parameters to maintain optimal humidity levels.
3. If a significant deviation occurs, initiate a deviation report (Annexure-1) and review the batch for any potential impact on tablet quality.
4. Take corrective actions to prevent future deviations, including equipment calibration, process adjustments, or procedural updates.

5.6 Acceptance Criteria

1. The batch is considered acceptable if the humidity levels in the manufacturing area remain within the specified range (typically 40% to 60% RH) during the critical phases of tablet production.
2. If deviations occur but corrective actions bring the humidity back within the acceptable range, the batch may still be accepted, provided there is no adverse impact on tablet quality.
3. If humidity levels remain outside the acceptable range for an extended period, initiate a full investigation and corrective action, which may include rework or rejection of the batch.

5.7 Post-Testing Actions

1. After the humidity levels have been adjusted and are within the acceptable range, continue with the next step in the tablet manufacturing process, such as drying, compression, or coating.
2. Ensure that all documentation is complete, including batch records, humidity logs, and corrective actions taken during the process.

6. Abbreviations

• SOP: Standard Operating Procedure
• GMP: Good Manufacturing Practice
• QC: Quality Control
• QA: Quality Assurance
• CAPA: Corrective and Preventive Action

7. Documents

1. Batch Record (Annexure-2)
2. Deviation Report (Annexure-1)

8. References

• USP <701> – Humidity Control Guidelines
• 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals (US FDA)
• European Pharmacopoeia (EP) – Environmental Control Standards for Manufacturing

9. SOP Version

Version: 2.0

10. Approval Section

	Prepared By	Checked By	Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Deviation Report

Deviation Date	Batch Number	Deviation Description	Corrective Action	Responsible Person
15/12/2025	Batch 001	Humidity levels exceeded the acceptable range	Adjusted HVAC settings and re-calibrated environmental controls	John Doe

Annexure-2: Batch Record

Time	Humidity Level (%)	Temperature (°C)	Action Taken
08:00 AM	50%	22°C	No action needed
12:00 PM	65%	22°C	Adjusted dehumidifiers

Revision History:

Revision Date	Revision No.	Revision Details	Reason for Revision	Approved By
01/01/2024	1.0	Initial Version	New SOP Creation	QA Head
01/02/2025	2.0	Updated humidity monitoring criteria	Improved control and documentation processes	QA Head