IHS In-Patient Pharmacy Setup
( USP )

Turnkey Sterile Compounding Solutions by Innovative Healthcare Solutions

Understanding USP

USP 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