Tag: Utilities & Support System Validation

Critical Alarms and Interlocks in HVAC Validation

Critical Alarms and Interlocks in HVAC Validation Critical Alarms and Interlocks in HVAC Validation The validation of heating, ventilation, and air conditioning (HVAC) systems is crucial in the pharmaceutical and biologics industries, where stringent regulations dictate the maintenance of controlled…

Validating Temperature and Humidity Controls in Clean Areas

Validating Temperature and Humidity Controls in Clean Areas Validating Temperature and Humidity Controls in Clean Areas Temperature and humidity controls in clean areas are critical components of pharmaceutical process validation, especially within the context of medium fill operations. This step-by-step…

Microbial Monitoring in HVAC Ducts and Return Vents

Microbial Monitoring in HVAC Ducts and Return Vents Microbial Monitoring in HVAC Ducts and Return Vents The validation of HVAC systems, specifically focusing on microbial monitoring, is a crucial aspect of ensuring the quality and safety of pharmaceutical products during…

HVAC System Monitoring Parameters: What to Track and Why

HVAC System Monitoring Parameters: What to Track and Why HVAC System Monitoring Parameters: What to Track and Why In the pharmaceutical industry, maintaining a controlled environment is critical for product quality, safety, and compliance with regulatory standards. HVAC systems play…

Writing an HVAC Qualification Protocol (IQ, OQ, PQ)

Writing an HVAC Qualification Protocol (IQ, OQ, PQ) Writing an HVAC Qualification Protocol (IQ, OQ, PQ) The HVAC system in pharmaceutical manufacturing is critical to maintaining the integrity of cleanroom environments. This comprehensive guide outlines the step-by-step process for developing…

HVAC Zoning and Pressure Cascade Validation in Controlled Environments

HVAC Zoning and Pressure Cascade Validation in Controlled Environments HVAC Zoning and Pressure Cascade Validation in Controlled Environments In the pharmaceutical industry, ensuring environmental integrity through proper HVAC (Heating, Ventilation, and Air Conditioning) zoning and pressure cascade validation is pivotal…

Air Change Rate and Recovery Time Calculations for HVAC Validation

Air Change Rate and Recovery Time Calculations for HVAC Validation Air Change Rate and Recovery Time Calculations for HVAC Validation In the pharmaceutical industry, ensuring high-quality production environments is critical to maintaining product integrity and compliance with regulatory standards. HVAC…

HEPA Filter Integrity Testing: DOP, PAO, and Beyond

HEPA Filter Integrity Testing: DOP, PAO, and Beyond HEPA Filter Integrity Testing: DOP, PAO, and Beyond HEPA filter integrity testing is a critical component in ensuring that cleanrooms and controlled environments in the pharmaceutical industry meet stringent regulatory standards. This…

How to Perform Airflow Visualization (Smoke Study) for Cleanrooms

How to Perform Airflow Visualization (Smoke Study) for Cleanrooms How to Perform Airflow Visualization (Smoke Study) for Cleanrooms Airflow visualization, often referred to as a smoke study, is an essential component of process validation in the pharmaceutical industry, particularly in…

HVAC System Validation in Pharma: Step-by-Step Guide

HVAC System Validation in Pharma: Step-by-Step Guide HVAC System Validation in Pharma: Step-by-Step Guide In the pharmaceutical industry, the validation of Heating, Ventilation, and Air Conditioning (HVAC) systems is crucial to ensure that environmental conditions for manufacturing processes are controlled…