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Accessories & consumables, Filling consumables

Single-use Systems

Custom single-use systems for sterile fluid transfer

Compatibility
Universal
Customization level
Customized
Single-use systems at a glance

Single-use assemblies tailored to your needs

  • Assured sterility

    Each assembly is sterilized or irradiated and ready-to-use

  • Process flexibility

    Assemblies can be tailored to specific workflows, from upstream processing to final filling

  • Batch adaptability

    We supply assemblies in the quantities you need, from small prototype lots to full-scale manufacturing runs

  • Process engineering

    Our specialists provide technical guidance to align assembly design with your process goals

  • End-to-end management

    We manage the entire lifecycle, from supplier selection and component sourcing to assembly, packaging, and final release

  • Regulatory compliant production

    Production in ISO 5- and ISO 7-certified cleanrooms

  • Flexible validation

    Different validation methods available

  • Experienced team

    More than 20 years of experience in the field of single-use assemblies

Application

Flexible areas of application

  • For aseptic fill and finish

    Reliable product path for filling of vials, syringes, or cartridges.

  • For sampling

    Secure and sterile sampling connections for in-process control and quality testing.

  • For filtration and distribution

    Integrated solutions for sterile filtration, buffer/media preparation, and controlled fluid distribution across processing steps.

  • For sterile bag systems

    Configurable sterile bags for safe storage, transport, and handling of liquids or intermediates.

Process

How it works

  • 1

    Goal and process definition

    You define your assembly needs.

  • 2

    Internal alignment

    We align requirements with process feasibility.

  • 3

    Creation of prototype

    Together we develop a bespoke, single-use prototype.

  • 4

    Prototype validation

    You validate the prototype in your process.

  • 5

    Manufacturing

    We handle manufacturing, packaging, and sterilization.

Product highlights

Transforming your requirements into solutions

  • Batch adaptability

    From prototypes to full-scale runs, we supply the quantities required at each product development phase. This ensures you always have the right assemblies to match your process.

  • Process engineering

    With more than 20 years of single-use expertise, we guide you to achieve the performance you need while ensuring designs remain compatible with industrial manufacturing.

  • End-to-end management

    We oversee the complete project lifecycle: supplier qualification, material sourcing, assembly, sterilization or irradiation, packaging, quality control, and compliance monitoring. This guarantees reliable results and peace of mind for you.

Technical specifications

  • Production

    In ISO 5- and ISO 7-certified cleanrooms

  • Certification

    ISO 15378

  • Options

    Material gamma-irradiated or sterilized upon request

  • Release

    By a qualified person (QP)

  • Validation options

    Gamma sterilization, transportation, endotoxins, bioburden, and particles validations

  • Contamination control

    Cleaned with filtered air purging

  • Overmolded assemblies

    High integrity sealing validated up to 2.5 bars

FAQs

  • They are adaptable to all critical aseptic fluid transfer steps, including filling, sampling, filtration, storage, and distribution. Assemblies are designed to support applications from research and development to commercial manufacturing.

  • Assemblies are produced in ISO 7 cleanrooms, sterilized (SAL 10-6) or gamma-irradiated, and released by a qualified person (QP). Comprehensive validations – covering integrity, endotoxins, bioburden, and transport – ensure compliance and reliability.

  • Yes. Each assembly is tailored in collaboration with your team. We co-develop prototypes, align them with process feasibility, and scale up to manufacturing while maintaining sterility and regulatory compliance.

  • Yes. The packaging was tested after a full isolator decontamination cycle, and no trace of H2O2 was found inside the packaging.

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Get in touch!

Whether you have a question about our products, need technical support or would like to find out more about our solutions.

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