Standard Operating Procedure for Environmental Monitoring in Aerosol Production
1) Purpose
The purpose of this SOP is to establish a standardized procedure for environmental monitoring in aerosol production. This ensures that the production environment is continuously monitored and controlled to maintain product quality and comply with regulatory requirements.
2) Scope
This SOP applies to all areas within the aerosol production facility at [Company Name], including cleanrooms, production areas, and storage areas.
3) Responsibilities
Quality Assurance (QA) Manager: Oversee the environmental monitoring program and ensure compliance.
Environmental Monitoring (EM) Team: Conduct environmental monitoring activities and report findings.
Production Manager: Ensure that production activities comply with environmental monitoring requirements.
All Personnel: Follow environmental monitoring procedures and report any deviations.
4) Procedure
4.1 Environmental Monitoring Plan:
4.1.1 Develop an Environmental Monitoring Plan (EMP) outlining the monitoring strategy, sampling locations, frequency, and methods.
4.1.2 Identify critical control points within the production facility where environmental monitoring will be conducted.
4.1.3 Define action and alert limits for environmental parameters such as particulate counts, microbial counts, and temperature/humidity.
4.2 Sampling Procedures:
4.2.1 Conduct air sampling using appropriate methods such as active air sampling and settle plates.
4.2.2 Perform surface sampling using contact plates or swabs to monitor microbial contamination.
4.2.3 Measure temperature and humidity levels using calibrated instruments at designated locations.
4.3 Monitoring Frequency:
4.3.1 Perform environmental monitoring at a frequency specified in the EMP, based on risk assessment and regulatory requirements.
4.3.2 Increase monitoring frequency during critical production activities or following significant changes in the production environment.
4.3.3 Conduct additional monitoring in response to deviations or out-of-specification results.
4.4 Data Analysis and Reporting:
4.4.1 Analyze environmental monitoring data to identify trends and deviations from established limits.
4.4.2 Document all monitoring results, including date, time, location, and analysis results.
4.4.3 Prepare regular environmental monitoring reports summarizing the findings and any corrective actions taken.
4.5 Corrective and Preventive Actions:
4.5.1 Investigate any deviations or out-of-specification results to identify the root cause.
4.5.2 Implement corrective actions to address the immediate issue and prevent recurrence.
4.5.3 Review and update the EMP and related procedures as necessary based on the findings.
4.6 Review and Approval:
4.6.1 The QA Manager reviews and approves all environmental monitoring reports and corrective actions.
4.6.2 The QA Manager ensures that all monitoring activities are documented and records are maintained.
4.6.3 Conduct periodic reviews of the environmental monitoring program to ensure its effectiveness and compliance.
5) Abbreviations, if any
QA: Quality Assurance
EM: Environmental Monitoring
EMP: Environmental Monitoring Plan
SOP: Standard Operating Procedure
6) Documents, if any
Environmental Monitoring Plan (EMP)
Environmental Monitoring Records
Calibration Records
Monitoring Reports
7) Reference, if any
GMP Guidelines
ISO 14644: Cleanrooms and Associated Controlled Environments
FDA Guidance for Industry: Sterile Drug Products Produced by Aseptic Processing
8) SOP Version
Version 1.0
