BIO supports biosimilars legislation.

Press Release Summary:



BIO and the Delaware BioScience Association commend Delaware State Senate for introducing legislation designed to address regulatory issues related to the interchangeability of biological medicines. Biosimilars are not generics, and even slight changes to biologic drug can change its properties entirely. Senate Bill 118 seeks to properly preserve physician-patient relationship, protect patient access to accurate prescription information, and promote competitive market for biologic therapies.



Original Press Release:



Biosimilars Legislation Introduced To Notify Patients of Changes to Prescriptions



Patients Should Be Notified if Doctor's Prescription Changed



WASHINGTON -- The Biotechnology Industry Organization and the Delaware BioScience Association (Delaware Bio) commend the Delaware State Senate for introducing legislation designed to address the regulatory issues related to the interchangeability of biological medicines.



The policies outlined in Senate Bill 118 align with BIO’s principles on biologic substitution, therefore BIO support passage of this bill.



While the U.S. Food and Drug Administration (FDA) oversees approval of biologic medicines, policies governing whether one product may be substituted in place of a doctor's prescription and whether a pharmacist must notify a consumer is covered by state law. Senate Bill 118 seeks to properly preserve the physician-patient relationship, protect patient access to accurate prescription information, maintain incentives for innovation and promote a competitive market for biologic therapies.



Biosimilars are not generics. Even slight changes to a biologic drug can change its properties entirely. Unlike conventional generic medicines, biosimilars are not the same as the drugs they seek to substitute. In fact, two biologics made using different cell lines and differing manufacturing processes will rarely, if ever, be exactly the same, hence the name “biosimilar.” Those suggesting biosimilars and generics are the same are wrong.



Patients and physicians managing chronic conditions are generally aware of which biologic treatments work best in their unique circumstances. Providing notice to patients and physicians allows everyone involved the opportunity to discuss past treatment experiences so that any possible negative issues can be better understood and avoided.



As the Delaware State Senate continues to address issues related to biosimilars, BIO and Delaware Bio encourage policy makers to continue to put patients first.



About BIO

BIO represents more than 1,100 biotechnology companies, academic institutions, state biotechnology centers and related organizations across the United States and in more than 30 other nations. BIO members are involved in the research and development of innovative healthcare, agricultural, industrial and environmental biotechnology products. BIO also produces the BIO International Convention, the world’s largest gathering of the biotechnology industry, along with industry-leading investor and partnering meetings held around the world. BIO produces BIOtechNOW, an online portal and monthly newsletter chronicling “innovations transforming our world.” Subscribe to BIOtechNOW.



Contacts

Biotechnology Industry Organization

George Goodno, 202-962-6660

Web: www.bio.org

Blog: www.biotech-now.org

Twitter: @IAmBiotech


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