Vita means life. It's also our platform for sharing the stories of biotech's promise to patients and public health.
CSL consists of CSL Behring, CSL Seqirus and CSL Vifor. Learn more by visiting each section.
Biotechnology leader CSL Behring offers the broadest range of quality plasma-derived and recombinant therapies in our industry.
Derived from the expression 'securing health for all of us', CSL Seqirus is one of the world's largest influenza vaccine providers.
R&D focuses its expertise on four strategic platforms: plasma protein technology; recombinant technology; cell and gene therapy; and vaccines technology.
One of our core values at CSL is Innovation. We support collaborative innovation through the endowment of awards and grants to researchers around the world.
As part of our broader sustainability strategy to build a more sustainable future, CSL commits to reduce absolute Scope 1 and 2 greenhouse gas emissions by 42% by FY2030.
Along with our sustainability strategy, CSL’s community contribution framework helps deliver on our Values and support execution of our 2030 strategy.
At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out.
Whether you are early in your college education or recently completed your degree, it's never too soon to consider CSL for your Promising Future!
For decades, the rare disease Hereditary Angioedema (HAE) overwhelmed Melissa’s days. But today she’s making up for lost time…
Makiko Matsuyama, president of Japan’s Hereditary Angioedema (HAE) patient association, discusses the danger of undiagnosed H…
Dr. Konrad Bork encourages the next generation of physicians to listen to their patients and stay curious. He’s been research…
An associate professor living with Hereditary Angioedema encourages fellow patients to “never give up and try to persist in y…
A rare condition, HAE, causes unpredictable swelling attacks that can be life-threatening. Day-to-day, patients live with the…
Kids in a rare disease research trial deserve extra care. That’s why CSL decided to be the first ever to provide “Clinical Co…
Their condition is so little known, patients who live with hereditary angioedema (HAE) endure diagnostic delays characterized…
A high school senior, Jack recalls more than a decade of swelling attacks due to hereditary angioedema, including a life-thre…
Lexi lives with the rare disease hereditary angioedema (HAE). She reflects on how the condition’s random swelling attacks imp…
The U.S. Hereditary Angioedema Association (HAEA) and HAE International (HAEi) offer fun, educational and empowering programm…
To better understand how patients experience hereditary angioedema (HAE), CSL invited Anthony Castaldo and Henrik Boysen to m…
Test your knowledge of hereditary angioedema, a rare disease that causes unpredictable swelling.
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