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.

Learn more about inclusiv Modular Cleanrooms

Contact our experts to discuss your sterile compounding needs and plans for the future.