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Cleanroom approach
The manufacturing plan is matched to component risk and customer requirements.
- Controlled access
- Personnel gowning
- Segregated workflow
- Material control
- In-process inspection
- Clean packaging
Controlled manufacturing
Class 100,000 cleanroom production for hygiene-sensitive projects.
Segregated workflows, controlled handling and traceability support medical and other applications with defined cleanliness requirements.
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Project planning
Cleanroom production is one part of the complete validation and quality plan.
- Application classification
- Material documentation
- Process definition
- Inspection plan
- Packaging requirements
- Traceability expectations
Documentation by application
Confirm the exact grade, test scope and intended use.
Technical data and compliance documentation are supplied according to the selected material or product. We do not treat one test report as universal approval for every formulation.
Review our quality approachStart a technical conversation
Discuss a medical silicone project.
Our team will review your requirements and recommend an appropriate material, process and development path.