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Medical Device Packaging

With the most comprehensive packaging testing services in Europe for ISO 11607, we can meet all the tests for medical device packaging needs in one location.

ISO 11607-1 specifies the requirements for materials and test methods, pre-formed sterile barrier systems, sterile barrier systems and packaging systems that are intended to maintain sterility of terminally sterilized medical devices until the point of use.

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Our services in Package Testing area include:

ISO 11607-2 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include the forming, sealing and assembly of pre-formed sterile barrier systems, the sterile barrier systems themselves and the packaging systems.

Our services in ISO 11607-2 include:

  • Consultancy
    • Process development
    • IQ – OQ – PQ
  • Test Plans and Protocols
  • Sampling
  • Validation Testing
  • Technical and Regulatory Files
  • Comparative performance studies
  • Packaging system analysis

All under the auspices of our ISO 17025 accreditation.

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Case Study – Emerson Network Power

Case Study

Emerson Network Power logo

How Anecto developed a number of innovative solutions for the leading multinational Emerson Network Power.