Robidoux's reelection comes as biosimilars get a lift from automatic switching policies in British Columbia and Alberta.
Biosimilars Canada, a national trade association representing biosimilar developers and other industry stakeholders, has reelected Michel Robidoux, the president and general manager of Sandoz Canada, to serve as chair of the Biosimilars Canada board.
In a statement announcing his reappointment, Robidoux praised the biosimilar switching policies implemented by British Columbia and Alberta in 2019. These policies require that patients with chronic conditions be transitioned to certain biosimilars under the oversight of their physician. The programs have achieved savings that proponents have said could be reinvested in health care to broaden access not only to biologics but also other therapies and services.
“Biosimilar medicines have an important role in supporting health care sustainability and patient care,” Robidoux said. “The implementation of biosimilar switching policies could save the Canadian health care system hundreds of millions of dollars.” Citing a 2020 report by the Ontario Drug Policy Research Network, the statement said that annual savings of $425.6 million for provincial drug plans is possible in Canada by switching patients from 3 of the top-selling reference biologics: Humira (adalimumab), Enbrel (etanercept), and Remicade (infliximab). “A similar magnitude of savings would be available for employer-sponsored benefit plans,” it said.
Biosimilars Canada is affiliated with the European trade group International Generic and Biosimilar Medicines Association and is a division of the Canadian Generic Pharmaceutical Association. The group also reelected Mike Woolcock to serve as vice chair of the board. Woolcock is a senior vice president at Apobiologix. Other companies represented by Biosimilars Canada include Auropharma, Fresenius Kabi, Pharmascience, Taro, Teva, and Viatris.
For an update on biosimilar savings in British Columbia from the perspective of Pacific Blue Cross, click here.
Boosting Health Care Sustainability: The Role of Biosimilars in Latin America
November 21st 2024Biosimilars could improve access to biologic treatments and health care sustainability in Latin America, but their adoption is hindered by misconceptions, regulatory gaps, and weak pharmacovigilance, requiring targeted education and stronger regulations.
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.
Eye on Pharma: EU Aflibercept Approvals; Biosimilars Canada Campaign; Celltrion Data
November 19th 2024The European Commission grants marketing authorization to 2 aflibercept biosimilars; Biosimilars Canada launches new campaign to provide sustainable solutions to employers; Celltrion shares positive data for 2 biosimilars.
Can Global Policies to Boost Biosimilar Adoption Work in the US?
November 17th 2024On this special episode of Not So Different honoring Global Biosimilars Week, Craig Burton, executive director of the Biosimilars Council, explores how global policies—from incentives to health equity strategies—could boost biosimilar adoption in the US.
Breaking Down Biosimilar Barriers: Interchangeability
November 14th 2024Part 3 of this series for Global Biosimilars Week, penned by Dracey Poore, director of biosimilars at Cardinal Health, explores the critical topic of interchangeability, examining its role in shaping biosimilar adoption and the broader implications for accessibility.