IHS In-Patient Pharmacy Setup
( USP )

Turnkey Sterile Compounding Solutions by Innovative Healthcare Solutions

Understanding USP

USP <797> ensures safe compounding of sterile preparations (CSPs).

Prevent microbial contamination

Establish environmental controls

Ensure personnel training

Maintain rigorous cleaning protocols

Compliance is essential for all sterile compounding operations.

Cleanroom Design & Infrastructure Key Technical Requirements: - ISO Classifications:

Buffer Area: ISO 7

Ante Area: ISO 8 or better

HEPA-filtered airflow with positive pressure

Smooth, cleanable surfaces

Temperature < 20°C, controlled humidity

Regular certification and monitoring

Personel & Operational Protocols

Comprehensive training in aseptic technique

Proper garbing: gowns, gloves, masks, shoe covers

Hand hygiene enforcement

Surface disinfection with sterile 70% IPA

Minimized traffic to reduce contamination risk

IHS Turnkey Solutions

Complete Pharmacy Setup Support:

Custom design and engineering- Custom design and engineering

Modular cleanroom construction

Laminar airflow & biosafety cabinet installation

Environmental validation and documentation

Regulatory inspection readiness

IHS InPatient Pharmacy Gallery Images