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Aseptic Liquid Transfer using a DPTE® Alpha Port and a DPTE-BetaBag®

How to speed up aseptic liquid transfer while maintaining sterility?

The single-use DPTE-BetaBag® is playing an increasingly important role in scale-up and high-speed manufacturing operations by providing an aseptic liquid transfer solution that delivers on safety and sterility. Especially in final filtration and filling operations, maintaining sterility throughout the entire process is critical.

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Proving leaktightness of the DPTE® system

The DPTE® system is the industry benchmark for secure sterile transfer in pharmaceutical production. It reduces manual intervention and so lowers contamination risk. Learn more about a tried and tested method to minimize microbial contamination while keeping up the pace in production.

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Four DPTE-BetaBag® Tyvek filled with components ready to be sterilized

Optimized Handling of DPTE-BetaBag® Tyvek® in steam sterilization

Following specified load and autoclave cycle parameters will result in the best performance for DPTE-BetaBag® Tyvek®. These easy steps will improve outcomes and reduce the risk of bag failure. Understand how the performance of the DPTE-BetaBag® Tyvek will be optimized by using proper procedures.

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Secure requalification with the DPTE® system

The Original DPTE® system from Getinge is the world's leading sterile transfer solution. A fully validated system, DPTE® enables you to efficiently secure requalification in your production. Discover a breakdown of the advantages.

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An operator docking a DPTE-BetaBag® filled with caps to a DPTE® Alpha port

Which DPTE® solution is best for you?

The Original DPTE® system from Getinge is the world's leading sterile transfer solution. A fully validated system, DPTE® is available with both single-use DPTE-BetaBag® and reusable Beta Containers to match your needs. Learn more about the advantages of each solution.

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Transfer of components using a DPTE-BetaBag® and a DPTE® Alpha Port

Improving industry-standard DPTE-BetaBag® validation

Educated in the Control and Development of Pharmaceutical Products, Sophie Corbineau worked in pharmaceutical production for eight years, before joining Getinge as a Validation Expert in 2015.

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Meeting standards and exceeding production for DPTE-BetaBag®

Since beginning her career as an Operator in the 1990s, Cleanroom Supervisor Karine Piquot has studied every aspect of cleanroom production at Getinge.

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Operator using a DPTE® Alpha port for sterile transfer

The benefits of the complete DPTE® system

The original DPTE® system from Getinge is the world's leading sterile transfer solution.The most important advantage of using both DPTE® Alpha and DPTE® Beta components is that as one complete system it is validated by Getinge.

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An operator using the DPTE® Transfer Trolley to connect a DPTE-BetaBag® to a DPTE® Alpha port

The origins of the original DPTE®

Part of Getinge since 2005, La Calhene has been a pioneer in containment and aseptic transfer technology for nearly six decades.

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Operator connecting a DPTE® Beta Container to a DPTE® alpha port

Applying the DPTE® transfer system to a Glovebox

Getinge’s DPTE® Beta containers are used, amongst other applications, for safe and leak-free transfer of highly potent active pharmaceutical ingredients (HPAPI).

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Operator doing some manipulations in a filling line

Getinge and IMA Life create flexible solutions for the pharma and biopharma industries

In some projects IMA Life works together with Getinge to find advanced solutions to meet the most demanding customer needs.

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Operator working in a drug manufacturing

Containment of APIs released through component washing

Personnel and environmental safety are critical for pharmaceutical companies that manufacture drugs with hazardous or potentially hazardous Active Pharmaceutical Ingredients (APIs). APIs are a normal byproduct of pharmaceutical production, research and development that can be released into the loading and service area via the component cleaning/washing process.

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5월 2022

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