Pharmaceutical Clean Room Design & Construction

As a nationally recognized leader in pharmaceutical clean room innovation, Precision Cleanrooms® is a one-stop source for world-class design-build modular clean room services.

The pharmaceutical cleanrooms industry is heavily regulated, and pharmaceutical clean room environments must conform to rigid regulations and precise measures to achieve a high level of success and sustainability. Precision Cleanrooms is a turnkey design/build manufacturer of pharmaceutical cleanrooms with a full understanding of these mission-critical specifications.

What sets us apart from the competition is a winning combination of flexible and scalable solutions, our interactive design philosophy and a performance guarantee. We offer full turnkey engineering, design and construction solutions for your pharmaceutical clean room project.

Pharmaceutical Clean Room Company

  • Modular Pharmaceutical Clean Room Design & Assembly

    Our pharma cleanrooms are designed and pre-fabricated using industry-proven protocols and specification. A site supervisor maintains clean on-site assembly and efficient installation. Our cleanroom installation crews travel nationwide and construct your cleanroom to predetermined schedules until the pharma cleanroom project is complete through certification. Our goal is to design and construct cleanrooms to enhance your business productivity.

  • Expandable Pharmaceutical Cleanroom Structures

    Our pharma cleanrooms are truly modular and can be expanded or modified as needed with minimum downtime and interruption to your business activity.

  • Pharmaceutical Cleanroom Customization

    With Precision Cleanrooms we off­er ISO Class 3- to 8-rated cleanrooms, as your specifications require, with certification services available. Our seismic-zone rating and structural integrity will meet or exceed the building requirements for your city and state.

  • Turnkey Pharmaceutical Cleanroom Offering

    Our business model caters to comprehensive projects addressing all 17 construction divisions. Our interactive design philosophy allows us to deliver pharma cleanroom solutions with energy efficient operations and long-term life cycles.

  • Performance Guarantee

    We guarantee that our pharmaceutical cleanrooms meet your project requirements and exceed your expectations for quality and service.

  • Our cleanroom designs are compliant to cGMP standards, GMP European Standards for Sterile Injectables and/or FDA cleanroom standards.

  • Precision Cleanrooms’ control systems are compliant to FDA CFR 21 Part II.

Pharmaceutical Cleanroom Services:

Precision Cleanrooms offers full-service turnkey pharmaceutical cleanrooms including:

  • Cleanroom Consultation

  • Cleanroom Budgeting and Planning

  • Cleanroom Design and Engineering

  • Cleanroom Construction and Assembly

  • Cleanroom Certification

  • Cleanroom Preventative Maintenance

Cleanroom Gallery

FAQs About Pharmaceutical Clean Room

Pharmaceutical cleanrooms are subject to harsh chemical cleaning of both flooring and walls. Fiber Reinforced Plastic (FRP) walls have good chemical resistance are a common choice.[Learn more]
USP797/800 pharmaceutical cleanrooms are used for compounding drugs at pharmacies. Recommendations come from the USP however final authority lies with state pharmacy licensing boards. USP797/800 pharm[Learn more]
Pharmaceutical cleanrooms require both viable and non-viable particle testing. The viable testing is done with settling plates. The non-viable testing is done with laser particle counters.[Learn more]
Pharmaceutical cleanroom flooring must be chemical resistant, otherwise the aggressive cleaning agents used in pharmaceutical cleanrooms will damage the flooring. The cleanroom flooring minimize join[Learn more]
The FDA mandated CGMP Current Good Manufacturing Practices for pharmaceutical manufacturers which is a higher standard than GMP Good Manufacturing Practices. This is a higher standard for pharmaceutic[Learn more]
Pharmaceutical cleanrooms typically are ISO-5/class 100 for aseptic filling and sterile processes. Less critical area are often ISO-6/class 1000 or ISO-7/class 10,000. The EU GMP Annex puts similar bu[Learn more]