Modular Cleanroom Construction Process
We accompany you throughout the process until the final certification is granted.
Needs Assessment
Contact us to tell us about your needs.
Planning
Gather requirements, review current and desired operations and workflow.
Layout
Preliminary drawings reviewed, revised, and approved by stakeholders.
On site Construction
Project management, trades coordination, and installation.
Environmental Monitoring
Calibration, training, and activation.
Certification
CETA certification by an impartial third-party.
Conceptual and Detailed Cleanroom Design
inclusiv Cleanroom materials and accessories are suitable for use in positive or negative pressure environments.
- Facility assessment, design consultation, and workflow analysis
- Cleanroom air balance compliance
- Gap analysis and review of pharmacy operations
- Guidance and support for your mechanical engineers
- Engineering support, structural calculations, and drawings needed for Office of Statewide Health Planning and Development (OSHPD) submissions
Environmental Monitoring System
inclusiv Cleanroom design and installation includes an advanced monitoring system for:
- Particle count
- Temperature
- Humidity
- Pressure
Certification
Grifols guarantees that all our cleanrooms will pass Controlled Environment Testing Association (CETA) certification.
Need help with your sterile compounding plans?
Contact our experts to discuss your sterile compounding needs and future plans. Our team is here to support you.
Learn more about inclusiv Modular Cleanrooms
Modular Cleanrooms Specifications
Promote safety and compliance in the design, construction, and environmental.
Cleanrooms Certification
Grifols offers Cleanrooms compliance with USP <795>, <797>, and <800>.
Case Study: USP Compliance Cleanrooms
Cleanrooms Renovation for USP <797> and USP <800> Compliance
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