Ensuring contamination-free and scalable processes

Ensuring contamination-free and scalable processes while fulfilling the strictest compliance requirements

As a partner in pharmaceutical production, Getinge’s portfolio of biopharmaceutical resources meets our customers’ unique challenges and strict compliance requirements while achieving high performance, maximum productivity and streamlined processes. We produce GMP washers, sterilizers, closure processing systems, isolators, sterile transfer systems and bioreactors systems to meet each facility’s specific needs.

Discover how Getinge can support in contamination prevention and upstream bioprocessing for your specific application within the biopharmaceutical production space.

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Our solution to your needs

We support every step of your journey
From Science to Life

We help scientists and engineers move from idea to innovation.
From threat to cure. From science to life.

By leveraging our deep application know-how and global footprint, Getinge partners with scientists and engineers to develop and manufacture better pharmaceuticals.

We focus on contamination prevention and upstream bioprocessing to provide tailored, efficient and compliant solutions to our customers and partners who are dedicated to prevent, mitigate and cure diseases - saving lives.

Striving for the highest quality outcome from production processes

Biopharmaceutical production facilities are acutely concerned with maximizing uptime and performance while safeguarding against microbial and particulate contamination.

To ensure safety, all biopharmaceutical production facilities must comply with strict regulations. These include Good Manufacturing Practices (cGMP) associated with production of the finished product, and Good Laboratory Practices (cGLP) associated with quality testing related to the product. Each process and cycle must follow validated customer requirements to deliver stable and repeatable results in the shortest time and at a minimum cost.

Remote Factory Acceptance Tests (FAT)

To support our customers we use remote FAT as an alternative approach to performing Factory Acceptance Tests.

Complementary to our physical Factory Acceptance Tests, we offer remote FAT to continue to support you even in times of (travel) restrictions.

Download the remote FAT leaflet

Solutions tailored to your every need

We design and provide tailored, efficient, and compliant solutions based on our extensive portfolio and experience from +25,000 customers worldwide.

Worldwide presence and experience

Getinge’s worldwide reach, +10,000 employees, and extensive installed base in +135 countries give us the ability to support you anywhere in the world.

A century of application know-how

By leveraging our deep application know-how and global footprint, we partner with scientists and engineers to develop and manufacture better pharmaceuticals.

Our Service Team is always by your side

With our own Service Team by your side, you are ready to meet the requirements of accrediting organizations and government regulatory agencies.

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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.

Pharmaceutical Production

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.

Pharmaceutical Production

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.

Pharmaceutical Production

Sterile production of life-saving vaccines and medicines