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Hold deg oppdatert på kunnskapen fra Getinge

Abonner på nyheter om livskunnskap

Abonner på nyheter om livskunnskap

A scientist in protective gear works at an isolator with gloved ports in a laboratory setting.

Selecting the right equipment for aseptic processing

During sterile manufacturing, human operators pose the greatest risk for product contamination. To reduce microbiological and particulate contamination risks, aseptic techniques typically rely on either laminar flow equipment used within a cleanroom environment or barrier technology. Laminar flow equipment includes laminar flow hoods and biosafety cabinets (Class I, Class II, and Class III). Barrier technology includes restricted access barrier systems (RABS) and isolators.

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SUPR 250 Liter with ProControl and operator in cleanroom

Aragen's Validation Journey with Getinge's SUPR Single-Use Bioreactors

Aragen’s goal was to see if their production process could be easily scaled up to larger, single-use bioreactors. Learn more about their findings.

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Rubber components transferred in a filling line using the DPTE® System

4 key trends in sterile component transfer

Explore the future of pharmaceutical manufacturing with 4 key trends in sterile component transfer. From pre-validated solutions to manufacturing flexibility and increased automation, discover how industry leaders Getinge and West are shaping the landscape.

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DPTE® containment performance assessment

Effective containment solutions for potent APIs

Discover how our DPTE® rapid transfer port, tested in collaboration with SafeBridge® Regulatory & Life Sciences Group, ensures personnel and environmental safety in pharmaceutical manufacturing facilities. Read the assessment of containment performance, validating the effectiveness of the DPTE® Alpha port against potentially hazardous active pharmaceutical ingredients.

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DPTE® Alpha Port - The original Rapid Transfer Port since 1963

Celebrating 60 years of the original rapid transfer port

The pharmaceutical industry constantly seeks innovations that enhance the safety, efficiency, and precision of drug production. One such revolutionary technology that has significantly impacted the industry is the DPTE® system, introduced in the 1960s. This article explores the history and evolution of DPTE®, highlighting its pivotal role in pharmaceutical production and the extensive experience that Getinge brings to the table after 60 years in the field.

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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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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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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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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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Scientists in blue protective suits work in a cleanroom with stainless steel tables and shelves.

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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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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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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A lab technician in blue protective gear operates a machine in a clean room.

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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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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Person in protective gear operates a large stainless steel machine in a sterile laboratory environment.

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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er varemerker eller registrerte varemerker som tilhører Getinge AB, dets datterselskaper eller tilknyttede selskaper │ Alle rettigheter forbeholdes.

oktober 2024

Denne informasjonen er utelukkende ment for helsepersonell eller andre fagpersoner og er bare til orientering. Den er ikke uttømmende og erstatter derfor ikke bruksanvisningen, servicehåndboken eller medisinsk rådgivning. Getinge er ikke ansvarlig for det andre parter gjør eller ikke gjør på bakgrunn av dette materialet, og brukeren bærer risikoen for sin bruk av materialet.

Det er ikke sikkert behandlinger, løsninger eller produkter som nevnes i materialet, er tilgjengelige eller tillatt i det landet hvor du bor. Informasjonen kan verken helt eller delvis kopieres eller brukes uten skriftlig tillatelse fra Getinge.

Denne informasjonen er ment for et internasjonalt publikum utenfor USA.

De synspunkter, meninger og påstander som kommer til uttrykk, tilhører kun de intervjuede. De gjenspeiler eller representerer ikke nødvendigvis Getinges synspunkter.