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Dr Steven Yates Weighs How Relationships Between Nurses, Patients Influence Biosimilar Acceptance
Steven Yates, MD, explains how the relationships that nurses have with patients can influence biosimilar acceptance.
The Center for Biosimilars® interviewed Steven Yates, MD, a medical oncologist and medical director at Intermountain Healthcare in Las Vegas, Nevada. Three years ago, Intermountain hired him to lead its biosimilar adoption effort.
Dr Yates explains how critical nurse navigation is for all aspects of oncology, which can make explaining clinical and symptom information to patients easier. He said that nurses can be a valuable resource for patients for explaining complicated concepts, especially in regard to treatment selection. Yates also discussed his experience with the nurse navigators at his practice and how patients have an easier time contact them than their providers. Nurse navigators can allow for patients to be more in touch and informed on their care needs between office visits. Yates said it's important for patients receiving oncology therapy to be in contact with health care institutions in some capacity and that nurse navigators can also keep providers informed on any issues the patient is experiencing.
Enhancing Adoption of Infused Biosimilars for a Sustainable Future
October 30th 2024An IQVIA report highlights challenges to the sustainability of infused biosimilars in the US, citing rebate walls and reimbursement policies, and proposes key solutions to enhance adoption and benefits for all stakeholders.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Strengthening the Supply Chain: Key Insights From FDA Commissioner Dr Robert Califf
October 25th 2024At the GRx+Biosims conference, FDA Commissioner Robert Califf, MD, stressed the urgent need for data transparency in the global supply chain and the role of collaboration and artificial intelligence in ensuring the resilience of biosimilar and generic drug production.
FDA and Industry Experts Unpack Biosimilar Device Requirements
October 23rd 2024At the GRx+Biosims 2024 conference, a panel of industry experts and FDA officials discussed evolving device requirements for biosimilars and interchangeable biosimilars, highlighting new approaches to comparative use human factors studies, regulatory challenges, and alternative validation methods.
