ISO 7 Cleanroom Injection Moulding Services

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ISO 7 Cleanroom Injection Moulding Services

Nordell’s ISO Class 7 Cleanroom provides a certified, tightly controlled production environment for components where cleanliness, precision, and regulatory compliance are essential.

Designed for medical, pharmaceutical, diagnostics, electronics, and aerospace applications, our cleanroom delivers consistent, high-quality moulding for parts that cannot risk contamination.

Cleanroom production is best suited to projects where the required level of environmental control is defined by regulation, validation, product safety, or contamination-critical performance.

Located within our 40,000 sq ft facility in Worthing, West Sussex, the cleanroom integrates advanced filtration, environmental monitoring, and high-speed electric moulding presses, ensuring stable, repeatable production at medium and high volumes.

If your project requires elevated environmental control but not full ISO classification, our White Room Moulding services might be more suitable.

Contact our team today to learn more about our cleanroom services.

Benefits of Cleanroom Injection Moulding

  • Certified ISO 7 ControlValidated conditions for regulated and contamination-sensitive components.
  • Compliance & TraceabilityIdeal for medical, pharmaceutical, and safety-critical applications.
  • High-Reliability ProductionCleaner processing for fewer defects and consistent performance.

What Cleanroom Injection Moulding Enables

Nordell’s cleanroom supports applications where sterility, particle control, or environmental stability directly impact safety and performance.

It is ideal for products such as:

  • medical consumables and diagnostic components
  • pharmaceutical and life-science parts
  • sensitive electronics and optoelectronic housings
  • aerospace and high-reliability assemblies

These components require moulding environments that prevent contamination, protect functional surfaces, and maintain strict process control.

Further Reading: What Can Be Manufactured in a Cleanroom Environment?

Stable, Reliable, Regulated Production

ISO 7 conditions enable:

  • reduced particulate contamination
  • strictly controlled moulding environment
  • consistent optical and surface quality
  • lower NCRs and reduced rework

This level of control is particularly valuable for medium and high-volume production where repeatability is essential.

Clean Assembly and Secure Packing

Beyond moulding, our cleanroom includes dedicated clean assembly and packing zones where components can be:

  • assembled
  • kitted
  • inspected
  • sealed

This keeps products protected through every stage of manufacturing.

Cleanroom Facilities and Technical Capabilities

Nordell’s cleanroom was purpose-built by Total Clean Air (TCA) using ULPA filtration and environmental control systems that maintain ISO Class 7 cleanliness across all operating conditions.

Cleanroom Highlights

  • ISO Class 7 certification
  • ULPA filtration with 60 air changes per hour
  • 99.999% particle capture efficiency
  • High-speed electric presses (100–120 tonnes)
  • Environmental monitoring (pressure, airflow, temperature)
  • Strict gowning and contamination-control protocols
  • Dedicated assembly and packing areas

These capabilities allow us to support demanding medical and technical applications with complete process consistency.

Further Reading: Our ISO 7 Cleanroom Standards

Nordell's cleanroom taken from an elevated position
Our ISO 7 Cleanroom: From conception to completion.

Cleanroom Injection Moulding: FAQs

Cleanroom moulding raises important questions around compliance, material suitability, and when ISO 7 classification is required.

These FAQs address the most common queries we receive from engineering, regulatory, and procurement teams evaluating cleanroom production options.

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Medtech Spinout of Imperial

I have worked with Nordell over many years on different products and industries. Nordell’s support on initial design input to delivery components, has been invaluable in achieving project timescales and deliverables. Knowledgeable staff, who proactively highlight areas for improvement, whether design or costs savings. Supporting development of components to tight timescales.

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Global Engineering Development company

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Nordell's team is always eager to embrace new challenges and explore unconventional approaches. Their can-do attitude and collaborative spirit have led to the development of groundbreaking solutions that have significantly advanced our pharmaceutical operations.
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Director
Pharmaceutical Company

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