Alliance for Safe Biologic Medicines Responds to Supreme Court Decision

June 28, 2012

WASHINGTON – Dr. Richard Dolinar, chairman of the Alliance for Safe Biologic Medicines (ASBM) issued the following statement in response to the Supreme Court ruling on the Affordable Care Act and its impact on the Food and Drug Administration’s (FDA) creation of a biosimilar pathway. “As biosimilar medicines are introduced into the U.S. in the […]

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ASBM Advisory Board Members Convene on Physician Notification

June 18, 2012

ASBM Chairman Dr. Richard Dolinar convened a working group of Advisory Board members to discuss the elements of a physician notification policy for biosimilars that prioritizes patient safety. Read the summary.

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ASBM Advisory Board Members Convene on Physician Notification

June 18, 2012

ASBM Chairman Dr. Richard Dolinar convened a working group of Advisory Board members to discuss the elements of a physician notification policy for biosimilars that prioritizes patient safety. Read the summary.

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About the FDA and Biosimilars

November 4, 2011

By Bruce Rubin MedPage Today Although politicians and patients may debate the benefits and drawbacks of the U.S. healthcare system, when it comes to inventing new medical technologies and discovering life-saving treatments, no other nation matches the U.S. in terms of innovation and delivery of care. One reason the U.S. is so successful is that […]

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Alliance’s Dolinar Headlines Boston Biosimilars Event

October 5, 2011

By Kathy Feegal Dr. Richard Dolinar, the Alliance’s chairman, was a keynote speaker at a biosimilars roundtable discussion in Boston, MA on October 5, 2011. The event was hosted by Northeastern University and was attended by numerous stakeholders from across New England, including the Massachusetts Medical Society, and patients groups such as the National Kidney […]

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Biologics and Biosimilars: What Patients, Physicians and Advocates Need to Know Access, Patient Safety and Emerging Policy Issues

September 28, 2011

The Alliance for Safe Biologic Medicines joined with the Virginia Biotechnology Association at an event to expore with patients, advocates, physicians and other healthcare providers the importance of maintaining patient safety as the U.S. FDA’s top priority while it works to establish a pathway for approval for biosimilar products.

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Developing the Nation’s Biosimilars Program

August 4, 2011

Developing the Nation’s Biosimilars Program Steven Kozlowski, M.D., Janet Woodcock, M.D., Karen Midthun, M.D., and Rachel Behrman Sherman, M.D., M.P.H. New England Journal of Medicine August 4, 2011 Biologic products developed over the past three decades and approved by the Food and Drug Administration (FDA) now provide important therapeutic options for a variety of serious […]

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July 13, 2011

BioFlorida BioFlorida Institute Florida BioDatabase Florida Bioscience Education and Training Resources Florida Biotechnology News Florida Department of Health Florida House of Representatives Florida Institute of Technology Florida Medical Association Florida State Legislature Florida State Senate Office of Governor Rick Scott

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July 13, 2011

BioFlorida BioFlorida Institute Florida BioDatabase Florida Bioscience Education and Training Resources Florida Biotechnology News Florida Department of Health Florida House of Representatives Florida Institute of Technology Florida Medical Association Florida State Legislature Florida State Senate Office of Governor Rick Scott

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June 17, 2011

BaltimoreBio Biotechnical Institute of Maryland, Inc. Greater Baltimore Tech Council Johns Hopkins University Technology Transfer Maryland Biotechnology Center Maryland Department of Labor, Licensing and Regulation Maryland Department of Health and Mental Hygiene Maryland General Assembly Maryland Life Sciences Advisory Board Maryland Technology Enterprise Institute Office of Governor Martin O’Malley Tech Council of Maryland

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