- Complete turnkey clean room meets cleanliness standards for control of submicron particles, ensuring a clean compounding environment
- Exhaust containment system pulls air from compounding room to create negative-pressure containment of hazardous drugs, in accordance with USP 800 regulations
- Available with positive-pressure room for non-hazardous compounding, in accordance with USP 797
- Select ISO cleanliness level to suit your application: ISO 7 rooms for sterile-to-sterile compounding, or ISO 5 rooms for non-sterile-to-sterile compounding
- ISO 5 containment rooms comply with DQSA Section 503B for cGMP, FDA-resistered outsourcing operations
- Internal walls with swing doors creates a separate gowning ante-room
- Powder-coated steel support frame creates a rigid, durable structure that requires no external bracing or ceiling support
- BioSafe® interior Fiberglass-Reinforced Plastic (FRP) or C-PVC panels resist damage from physical contact, and stand up to IPA and other sterilizing agents
- Includes differential pressure gauges to simplify USP certification
|