Statement on IQVIA Report: Biosimilars in the U.S.: Reimbursement and Impacts to Uptake

Thursday March 25, 2021

WASHINGTON, DC (March 25, 2021) — U.S. patients rely on their health care providers to help them access biosimilars to treat their serious conditions. Today’s report reinforces the need and potential for straightforward policy proposals to encourage physicians in all settings of care to leverage biosimilar competition for their patients. We urge Congress and CMS to align Medicare payment policies to favor use of lower-cost biosimilars.

ATTRIBUTE TO: Christine Simmon, SVP Policy, AAM, Executive Director, Biosimilars Council

Read the full report here.

 

MEDIA CONTACT:
Rachel Schwartz
202.249.7147


About the Biosimilars Council

The Biosimilars Council, a division of the Association for Accessible Medicines (AAM), works to ensure a positive environment for patient access to biosimilar medicines. The Biosimilars Council is a leading source for information about the safety and efficacy of more affordable alternatives to costly brand biologic medicines. Areas of focus include public and health expert education, strategic partnerships, government affairs, legal affairs and regulatory policy. More information is available on our about page.

About AAM

AAM is driven by the belief that access to safe, quality, effective medicine has a tremendous impact on a person’s life and the world around them. Generic and biosimilar medicines improve people’s lives, improving society and the economy in turn. AAM represents the manufacturers and distributors of finished generic pharmaceuticals and biosimilars, manufacturers and distributors of bulk pharmaceutical chemicals, and suppliers of other goods and services to the generic industry. Generic pharmaceuticals are 90 percent of prescriptions dispensed in the U.S. but only 20 percent of total drug spending.

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The Council is involved in a number of events that focus on advancing biosimilars in the United States. Click on one below to learn more:

 

 

Registration Opens Soon. October 21–23, 2024 | Rockville, MD

GRx+Biosims™ 2024 is the leading regulatory science and policy event for the U.S. generics and biosimilars industry. Access the most recent information straight from experts at the Food and Drug Administration, grasp the latest policies shaping the industry, and acquire valuable insights to propel your professional development.