Usp 800 allows this but only for drugs that will be used for sterile compounding.
Usp 800 cleanroom design.
Usp 800 is a regulatory chapter issued by the united state pharmacopoeia.
General chapter 800 was published on february 1 2016.
To contain harsh drugs and contaminants in the lab the usp 800 door swings into the room.
Mecart is a north american turnkey design build cleanroom manufacturer with over 45 years of experience building world class cleanrooms.
It covers crucial standards and design requirements for the safe handling of hazardous drugs in pharmaceutical and healthcare environments.
Additionally a common commercial hvac system usually only achieves 4 to 6 acph.
Parallel designs provide the proper ante room requirements via cascading air systems.
This fails to consider the non sterile hazardous drugs which will need to be stored in a separate negative pressure storage room.
Usp 800 design requirements prioritize staff safety.
The current design of common commercial hvac systems are mostly inadequate for maintaining usp 800 s required acph engineering and iso clean air standards.
By transporting non sterile hazardous drugs through sterile spaces the pharmacy increases the risk of cross contamination.
Usp 800 context for implementation published 11 26 2019 compendial applicability of usp 800 published 11 18 2019 usp 800.
Review their work plan and past meeting summaries.
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Whisperflow laminar flow hood meets iso 5 primary engineering control requirement of usp 797.
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The usp compounding expert committee is responsible for the development of general chapter 800.
Cleanroom suite with usp 795 usp 797 usp 800 compounding areas.
Usp 800 clean room usp 800 hazardous drugs clean room design and construction by descco the united states pharmacopeial convention usp chapter 800 provides standards for handling hazardous drugs to promote patient safety worker safety and environmental protection.