Usp 797 Clean Room Temperature And Humidity Requirements

Low to medium risk.

Usp 797 clean room temperature and humidity requirements.

Secondary engineering control requirements by usp chapter 797 risk level low risk l ante area an iso class 8 see table 21 1 or cleaner area where personnel hand hygiene and. Practices28 31 32 and a discussion guide on usp chapter 797 17 and has recognized usp chapter 797 as a relevant practice standard in the ashp guidelines. Temperature and humidity requirements for the c sec room are lower than in the past. In june 2019 the united states pharmacopeia usp released several new and revised pharmacy compounding standards.

These requirements are addressed in usp 797 with revisions that call for a standard of a continuously maintained temperature of 20 degrees c 68 degrees f and 60 percent humidity. Revision as yet unproposed in pf of usp s definition for controlled room temperature from 20 25 to 2 30. Usp 797 changes with engineering controls removal of references to hazardous drugs defined temperature relative humidity requirements 20 c 68 f or cooler 60 rh no in room humidifiers or de humidifiers defined interval for environmental monitoring monthly 5. Minimum standard for pharmacies in hospitals.

Maintaining usp 800 s required acph engineering and iso clean air standards. Standards for prescribing preparation. Specifically usp published revisions to general chapter 797 pharmaceutical compounding and sterile preparations and published a new general chapter 800 hazardous drugs handling in healthcare settings. It describes a number of requirements including responsibilities of compounding personnel training environmental monitoring.

Personnel validation three consecutive media fill runs without contamination. Usp 797 guidelines minimum requirements for validation. Temperature and humidity gauges mounted in the room see appendix 1. 30 hours at room temperature 7 days at cold temperature and 25 days in a solid frozen state at 20 c or colder.

33 other professional organizations also provide guidance on specific aspects of compounding. 5 as described in usp chapter 797 for exposure of critical sites and must be in table 21 2. Usp 797 clean room guidelines standards. 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.