Let us help you educate your patients with bleeding disorders, through our comprehensive selection of professional educational materials.
Education for your patients.
Novo Nordisk helps you support your patients with resources and tools for success, right from the start. Educational materials available to download, share, or have delivered to your office.
Malcolm, center, lives with hemophilia A.
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Patient Brochure
This brochure describes key attributes of Novoeight®, with additional information on patient support and product support.
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Reconstitution Video
This patient-friendly educational tool shows both patients and HCPs how to correctly prepare Novoeight® for infusion.
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Conversation Starter
This 2-sided, 4-panel print piece is designed to help patients evaluate their treatment needs and show them how Novoeight® can meet those needs.
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Small Kit
Novoeight® is ready to go when they are. This stylish and customizable kit makes it easy to take up to a week’s worth of treatment on the go.
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Demonstration Kit
This kit demonstrates the compact storage size and portability of Novoeight®, and helps you show patients how quick it is to reconstitute a dose of Novoeight®. Patients may practice mixing a dose to become familiar with the process before leaving your office. Please see full Prescribing Information for complete Instructions for Use.
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Novoeight® is Ready To Go
Team Novo8™ member Vaughn chooses Novoeight® because its portability features support his active lifestyle. Share his story with patients looking for treatment options designed to fit their daily lives.
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Hemophilia Dictionary
This handy reference defines common terms used when talking about various bleeding disorders, with statistics and other facts that may help increase your patients’ understanding and awareness.
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Meet Our Representatives
Meet Steve, Jesús, and Tom, 3 Novo Nordisk Representatives who work directly with the hemophilia community. Hear about how Novo Nordisk has committed to addressing the community’s unique needs and how much they enjoy their role in helping to improve the lives of people living with hemophilia.
Education for you.
Patient advocacy groups.
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Hemophilia Federation of America™ (HFA)
Connecting people affected by bleeding disorders to others in their community, while advocating for the development of safe, affordable treatment options.
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National Hemophilia Foundation (NHF)
The largest nonprofit organization dedicated to education, advocacy, and research of inheritable bleeding disorders.
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World Federation of Hemophilia (WFH)
Committed to improving and sustaining excellent care for people with bleeding disorders across the world.
