BioNJ, the life sciences trade association for New Jersey, released a new white paper, “Prescription Drug Affordability Boards: Myths vs. Facts on Drug Supply Chain,” that corrects the record on several common myths about Prescription Drug Affordability Boards (PDAB) and their harmful impact on patients and the medical innovation ecosystem, according to the association.
The BioNJ white paper concludes that policymakers should avoid the creation of a PDAB as a means to control drug costs and should instead adopt solutions that will improve patient access and deliver savings to the health care system, such as capping patient out-of-pocket costs and using negotiated rebates to provide savings to patients.
“Prescription Drug Affordability Boards threaten patient access to existing treatments and dampen future medical innovations for hard-to-treat conditions,” said BioNJ President and CEO Debbie Hart. “BioNJ is committed to working with New Jersey policymakers to implement solutions that ensure Patients have meaningful access to their medicines, reduce health care costs, and support innovation necessary for future cures and treatments.”
The newly released BioNJ white paper provides background on the complex drug supply chain and addresses the ongoing concern that legislators across New Jersey and other states express: ensuring that their constituents have access to the latest and most effective therapies to help them manage medical conditions.
The BioNJ white paper addresses four specific misconceptions around the basis of using PDABs:
Download a copy of the white paper here.
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