Treating patients with hard-to-diagnose diseases requires a workforce with diverse experiences, perspectives and personal backgrounds that reflect patients and communities benefiting from our medicines. This #GlobalDiversityAwarenessMonth we recognize there's always more that can be done and will continue building on the progress we've made in creating an inclusive and equitable environment for our people, patients and partners. Learn more: https://bit.ly/3ZYlrqL
About us
Sobi is an international specialty healthcare company dedicated to developing treatments and extensive patient support networks for people with rare and difficult to treat diseases. These patients are often misunderstood, misdiagnosed and have limited medical options otherwise. This commitment has led to our world-class capabilities in protein biochemistry and biologics manufacturing, recognized by our leading industry partners. In North America, we have established our home bases in Waltham, MA and Toronto, Canada. Our employees not only have deep expertise in rare diseases, but are also dedicated to listening and learning from patients, payers and HCPs to ensure we’re bringing value to the region in the smartest, most impactful ways.
- Website
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http://www.sobi-northamerica.com/
External link for Sobi - North America
- Industry
- Biotechnology Research
- Company size
- 201-500 employees
- Headquarters
- Waltham, MA
- Type
- Public Company
- Specialties
- Inflammatory and genetic diseases and Rare diseases
Locations
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890 Winter Street
Waltham, MA 02451, US
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1155 North Service Rd. West
Unit #11
Oakville, Ontario Canada L6M 3E3, CA
Employees at Sobi - North America
Updates
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Busy days with an overflowing inbox and running from one meeting to the next. Sound familiar? On #WorldMentalHealthDay we understand the importance of creating a culture where leaders check in on their teams, colleagues check in on each other and where you check in with yourself. Checking in doesn't mean having all the answers, but it can encourage open dialogue and create a space where mental health is prioritized.
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We’re strongly committed to the communities we serve. That’s why the North America Medical Affairs team recently rolled up their sleeves and donated time during our annual medical meeting. Our team assembled hygiene packs with vital supplies to support Denver’s unhoused population, demonstrating our #rarestrength of care and making a meaningful impact on those in need.
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As victims in the southeast region of the U.S. continue to feel the devastation of #HurricaneHelene, we are supporting our disaster relief partner, American Red Cross, with a donation to provide needed supplies and medical care to the impacted communities. Our thoughts are with those affected by the storm and we urge everyone in the impacted areas to stay safe and be well.
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Know your blood counts! If you’re diagnosed with Myelofibrosis, your blood counts will play an important role in treatment. In your body, bone marrow is the factory for making blood cells. Myelofibrosis means scarring in the bone marrow. Complete blood counts (CBC) are the numbers a patient receives following a blood test analysis. This test looks at red and white blood cells and platelets. Doctors use your CBC -- whether it’s too high or too low -- to help determine your care. Learn more: https://bit.ly/4gIpmhj
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Today, our BIPOC ERG (V.O.I.C.E.) celebrated #HispanicHeritageMonth by hosting an inspiring conversation with Donna Baines, a mother of a Hemophagocytic Lymphohistiocytosis (HLH) warrior. Donna is a courageous caregiver who uses her platform to share her family’s experience with HLH to foster hope and motivate others to get involved. Thank you, Donna, for your passionate pursuit in bringing awareness to this tough to treat disease. #HistioAwarenessMonth
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This #HistioAwarenessMonth we’re breaking down this complicated disease into simple terms. What happens to a person living with hemophagocytic lymphohistiocytosis, better known as HLH? Put simply, something goes wrong with the macrophages, cells whose job is to clean up the mess in the human body. In a healthy individual the macrophages work together with red blood cells, but in a person with HLH, they cause damage by eating red blood cells and other healthy cells. Learn more: https://bit.ly/3Xut1GW
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#DYK only ten in every 100,000 people have immune thrombocytopenia (ITP), a rare autoimmune disease affecting platelet production? Until recently, treatment options were limited, but thanks to increased awareness of ITP, better outcomes are possible for people living with the disease. Learn more: https://bit.ly/4efp9R6 #ITPAwarenessWeek
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We’re not sure why patients develop myelofibrosis. For reasons we don’t yet understand, patients form mutations, and the genes that control how blood cells are made and how they act go awry. There’s nothing the patient did that caused it, but there’s a lot the doctors can do once they understand the mutation. Learn more: https://bit.ly/3ZPNatZ