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.
Getting Ready for Rare Disease Day 2022
On February 28, the global community of rare disease advocates will share their colors. Get tips on how to make the most of i…
Lighting the Night for Rare Disease Day
Landmarks around the world were illuminated on Sunday in honor of rare disease patients.
Take the Rare Disease Day Quiz
Test your knowledge about rare diseases, which affect more people than you think.
Learn, Interact and Celebrate
Rare Disease Day 2021 is happening amid a global pandemic. Here are three safe ways to take part.
CSL CEO Paul Perreault on Rare Disease Day
See the video Perreault shared with employees: “Reflect on the work we do and the people who count on us to keep innovating.”
Planning a Virtual Rare Disease Day
Rare disease advocates will log on this year to keep the cause front and center.
Show Your Stripes, Zebras!
Rare disease patients have adopted the zebra as an icon. Find out why.
A Spotlight on CIDP
Learn more about this rare neurological disorder.
Finding Purpose-Driven Work
Serving patients and working to protect public health weaves meaning into all roles at CSL, says our Chief Human Resources Of…
Watch: Why Rare Disease Day Matters to Us
Patients are “core to our DNA” so take time out to recognize them and their communities, says our Chief Medical Officer.
Meet Michael Joshua
Student, swimmer and Hemophilia B patient says his rare disease won’t hold him back.
Listen: Chasing the Cure
Doctor’s book tells story of researching his own rare disease.
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