With the Revised Schedule M, HVAC systems have gained renewed focus as a critical component in ensuring controlled environments, product quality, and regulatory compliance in pharmaceutical manufacturing. This course is designed to help engineering, validation, and QA professionals understand the updated expectations and practical steps for HVAC system qualification and monitoring.

Learn how to design, operate, and qualify HVAC systems that support cleanroom classifications, prevent cross-contamination, and maintain consistent environmental conditions across various dosage forms—sterile and non-sterile.

Stay audit-ready and technically sound with the knowledge to align your facility’s air handling systems with the latest CDSCO and international GMP guidelines.