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Cleanroom packaging by Strubl

Our range of cleanroom packaging products

All processes take place in encapsulated and monitored cleanrooms: tube film extrusion, bag manufacturing, manual manufacturing processes, and packaging. An integrated monitoring system ensures the quality of the cleanroom process.

Reinraumbeutel

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Reinraumfolien

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Cleanliner

Rundbodensäcke in Reinraumqualität

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Beutelsysteme

Mehrfachbeutel in Reinraumqualität

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Our range of services

  • Our modular system enables customized packaging design
  • Films, pouches, and bags in customer-specific designs
  • Special products: desiccant pouches, cross-bottom pouches, double-chamber bags
  • Competent process development ensures quality, cost-effectiveness, and speed in project implementation
  • Collective development of processes (quality assurance, organization, and logistics) and efficient, cooperative collaboration
  • TESTED DEVICE tested: our cleanroom packaging is suitable for cleanrooms up to cleanroom class ISO5

Protection against contamination

  • Cleanroom packaging prevents contamination risks
  • Packaging materials must meet the same quality standards as the end product
  • Films and bags from the cleanroom prevent contamination risks in the cleanroom process chain
  • Cleanliness and hygiene when used as primary and secondary packaging
  • Industries: Pharmaceuticals, medical technology. Supply industry, e.g., electrical/electronic parts, drives, hoses, pumps, valves, production equipment, cleanroom equipment

Cleanroom packaging from Strubl in the press

Cleanroom packaging in contamination-critical environments

(cleanroom & processes)

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GMP versus Packaging Ordinance

(Plastverarbeiter Medplast 05/24)

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Cleanroom packaging for protection against contamination

(ReinRaumTechnik 03/2023)

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Avoid contamination

(Reinraum Online - Das Reinraumportal Expertenpool 01/2023)

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GMP und Reinraumproduktion

GMP principles

  • Cleanroom production (ISO 14644-1, Class 8 and 9)
  • Hygiene management / Pest control / HACCP principles
  • GMP-compliant production processes, documentation, training
  • Traceability / process validation
  • Raw materials with EU Pharmacopoeia / FDA compliance
  • Contamination-free packaging (“bag-in-bag”), test certificates
  • ISO 9001:2008, EC error evaluation lists, in-process control

 

GMP processes

  • Extrusion (mono and coex)
  • Manufacturing
  • Manual manufacturing of special products
  • Packaging
  • Packaging (“bag-in-bag” for contamination-free transfer)

 

Pharmaceutical Packaging Working Group at IK

  • We are a member of the IK's Pharmaceutical Packaging Working Group, which aims to improve communication and cooperation in the pharmaceutical supply chain.