FDA Safety and Innovation Act (was: Creating Hope Act) signed into law today

From Yahoo:

WASHINGTON, July 9, 2012 /PRNewswire-USNewswire/ — Signed by President Obama today, theU.S. Food and Drug Administration (FDA) Safety and Innovation Act includes the most groundbreaking measures for rare disease patients and their families since the Orphan Drug Act of 1983. As the long-standing and recognized policy leader and advocate for the rare disease community, the National Organization for Rare Disorders (NORD) was instrumental in developing and shaping this legislation that includes provisions essential to patient access to safe and effective health care, issues critical to the rare disease community.
 
 
 
 
 
 
 
 
 
 
 
 
“This legislation represents true progress for people with rare diseases, who often face many struggles accessing treatments for their disorders,” said Peter L. Saltonstall, president and CEO of NORD. “Our heritage, understanding, leadership and commitment to the community uniquely position us to best understand the complexities and needs of people and organizations in the rare disease space. Today’s approval adds to NORD’s 30-year history of driving landmark legislation, which would not have been possible without the sustained efforts of our members and policy partners.”
 
Established in 1983 by patient advocates who successfully enacted the Orphan Drug Act, NORD has been an integral part of the development of the FDA Safety and Innovation Act since 2010. The Act will provide more than $6 billion in industry user fees to the FDA over the next five years to fund a share of the agency’s review of drugs and medical devices. Specific to the rare disease patient community, the Act provides the following:
— Accelerated patient access to new medical treatments — The development of Humanitarian Use Devices, or medical devices for small patient populations — Accelerated development of “breakthrough therapies”–those that show early promise — Enhanced consultation with rare disease medical experts — A rare pediatric disease priority review voucher incentive program — Addresses concerns related to conflict-of-interest regulations for advisory committee members
“We are grateful for the hard work and input our member organizations and policy partners have contributed over the past two years–raising awareness among Congress, the FDA and the National Institutes of Health. NORD looks forward to continued collaborations and to support the issues that deeply affect the rare disease community,” said Saltonstall.
 
About Rare Diseases
 
A rare disease is any disease affecting fewer than 200,000 Americans. There are nearly 7,000 such diseases–of which only about 250 have FDA-approved treatments–affecting nearly 30 million Americans.
 
About NORD
 
Established in 1983, the National Organization for Rare Disorders (NORD) is a unique federation of voluntary health organizations dedicated to helping people with rare “orphan” diseases and assisting the organizations that serve them. A nonprofit organization, NORD represents the 30 million Americans with rare diseases and is committed to the identification, treatment and cure of rare disorders through patient assistance, education, advocacy, research and service.
 
For more information, please visit www.rarediseases.org.
 

If you would like to read about the different bills that were included into this larger bill, including the Creating Hope Act, you can find a summary of them here: http://www.biotech-now.org/health/2012/07/fda-safety-and-innovation-act-a-monumental-step-forward-for-patients-with-rare-diseases

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