Usp 797 Clean Room Humidity Requirements

Ensure that your facility has a modern clean room environment.

Usp 797 clean room humidity requirements.

The following discussion describes considerations for functional operation of the suite cleanroom design usp requirements and basic hvac principles that must be carefully melded together to design and build a usp 797 suite that can be certified as compliant. Replace floors with seamless vinyl flooring. It describes a number of requirements including responsibilities of compounding personnel training environmental monitoring. And be at negative pressure between 0 01 and 0 03 inches of water.

Standards for compounding sterile preparations usp 797 helps to ensure patients receive quality preparations that are free from contaminants and are consistent in intended identity strength and potency. Favorable outcomes in usp 797 cleanrooms also require proper laminar flow workstation placement operator technique sanitation and room air cleanliness. United states pharmacopoeia usp 797 took effect on january 1st 2004 as a regulatory document which outlines procedures and environmental requirements for compounded sterile preparations csps. Adopt usp 797 facility engineering clean room guidelines.

Iso classification of particulate matter in room air particles 0 5 µm and larger per cubic meter iso class particle count 3 35 2 4 352 5 3 520 6 35 200 7 352 000 8 3 520 000. If the c sec for sterile compounding is a c sca the c sec should be externally vented. Implement a web based software system to ensure usp 797 compliance. To meet the updated usp 797 requirements photo courtesy of r c.

Usp 797 clean room guidelines standards portafab specializes in the turn key design and construction of modular clean rooms including applications specifically requiring usp 797 compliance. Install hepa filters in ceiling fans.