We are part of the CSL Limited group of companies. See how we're Driven by Our Promise.
We collaborate with rare disease organizations to promote quality medical care and services.
We offer a variety of support programs and activities for the patients we serve.
We also aim to make sure that nothing holds you back from getting the therapies you need.
Our product portfolio focuses on innovation in new products, improved products and manufacturing expertise.
A clinical trial is a research study that is done to find out if medical treatments can improve people’s health.
We work every day as if someone’s life depends on it, because it does.
We manufacture products to treat a number of rare diseases.
Help us deliver on our promise to save lives and protect the health of people.
Diversity and inclusion are top priorities for CSL Behring.
Construction began in 2020 and the 16-story building is almost complete. It’s a new anchor in the Parkville biomedical distri…
CSL Behring supports outreach to female neurologists in Japan to acknowledge the emotional weight of caring for patients and …
Go inside one of CSL’s manufacturing facilities in Bern, Switzerland, where the company recently launched a high-tech packagi…
After a harrowing journey to a hemophilia diagnosis for her son, Krissy is stepping up to help others.
Mom-to-be Danielle D. on overcoming her rare disease to live the life she has always envisioned.
The slow, deliberate martial art can relax your mind and take you beyond your physical limitations.
A person can mean well and still do some harm in the process. Watch this short video for tips that build connection.
Bzzzz! See a honeybee hive installation in this 60-second video.
New brand anthem film recognized alongside entries from the Smithsonian, Microsoft, ESPN and others.
The Beats Music Program from the Coalition for Hemophilia B brings patients together for a weekend of music training and perf…
CSL Behring’s partnership with a fly-fishing organization connects biotherapeutics leaders, veterans.
Video: Cheryl describes her journey coping with the rare disease hereditary angioedema (HAE) and how it has impacted her fami…
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