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Our mission is to ensure the generation of accurate and precise findings.

Contact Us 80 Gravel Pike Building D Red Hill, PA 18076​ (267)-313-4534 MONDAY - FRIDAY 09:00 AM - 05:00 PM info@bpssu.com
ISO Class 7 Cleanroom

ISO Class 7 Cleanroom Manufacturing

Our single-use assemblies are manufactured in an ISO Class 7 cleanroom environment, providing controlled conditions for the production of bioprocess components used throughout upstream, downstream, filtration, fluid transfer, and final fill applications.

Environmental controls and established operating procedures help minimize contamination risk while supporting consistent production from lot to lot.

ISO Class 7 cleanroom manufacturing at BPSSU
What We Build

What We Manufacture in Our Cleanrooms

BPSSU cleanroom operations support a wide range of custom and standard single-use products, including:

2D and 3D Single-Use Bags
2D and 3D Single-Use Bags
Tubing Assemblies
Tubing Assemblies
Bottle Assemblies
Bottle Assemblies
Filtration Assemblies
Filtration Assemblies
Bioreactor Kits
Bioreactor Kits
Final Fill Assemblies
Final Fill Assemblies
Fill Line Manifolds
Fill Line Manifolds
Column Assemblies & Accessories
Column Assemblies & Accessories
Mixing Assemblies
Mixing Assemblies
Custom Fluid-Transfer Assemblies
Custom Fluid-Transfer Assemblies
Our Workflow

Controlled Assembly From Start to Finish

Each assembly follows defined manufacturing procedures designed to support repeatability and traceability throughout the production process.

1
Component Preparation
2
Assembly
3
In-Process Inspection
4
Pressure / Integrity Testing
5
Labeling
6
Packaging
7
Sterilization Prep

Depending on the project, our cleanroom workflow may include component preparation, assembly, in-process inspection, pressure or integrity testing, labeling, packaging, and preparation for sterilization. This gives customers a clear, documented manufacturing path from individual components to the finished assembly.

Documentation & Traceability

Clean manufacturing is only part of the process

BPSSU also maintains documentation designed to support customer quality systems and audit requirements. This can include:

  • Lot traceability
  • Material and component documentation
  • Certificates of Conformance
  • Assembly records
  • Inspection and testing documentation
  • Sterilization documentation (where applicable)
  • Customer-specific documentation requirements
Single-use bioprocess assemblies built in the BPSSU cleanroom
Our Specialization

Designed for Single-Use Bioprocessing

Our cleanroom facility is specifically oriented around single-use bioprocess assemblies, allowing our team to work with the tubing, connectors, bags, filters, bottles, and other components commonly used throughout biopharmaceutical manufacturing.

That specialization helps us support both established assembly designs and highly customized configurations.

Flexible Production

Flexible Production for R&D Through Commercial Programs

Not every customer needs the same production volume. BPSSU can support:

R&D and Process Development

R&D and Process Development

Small quantities and rapid design iterations for teams developing or refining a process.

Clinical Manufacturing

Clinical Manufacturing

Documented, repeatable assemblies for clinical-stage programs where timelines and supply continuity are critical.

Commercial Manufacturing

Commercial Manufacturing

Repeat production with controlled specifications, documentation, and lot traceability.

Quality Built Into the Process

Quality is not a final checkpoint

Our cleanroom manufacturing operates alongside BPSSU's broader quality systems and inspection processes. Rather than treating quality as a final checkpoint, we build verification and documentation into the manufacturing process itself.

Need a Custom Cleanroom-Built Assembly?

Whether you're replacing an existing single-use assembly, developing a new process, or looking for a more responsive manufacturing partner, our team can help you evaluate your application and build the right configuration.

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