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Food and Drug Administration Reauthorization Act is Signed into Law

Monday, August 21, 2017   (0 Comments)
Posted by: Cathy Harrington
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Oley joins NORD in acknowledging President Trump for signing the Food and Drug Administration Reauthorization Act (FDARA) of 2017 into law.  This law makes it possible for the FDA to continue to review orphan drugs, biologics, and medical devices expertly, quickly, and safely. There are also critical improvements to the FDA's review of orphan therapies and medical devices factored in.

 

It takes a village and Oley is proud to serve as a member of NORD and collaborate on initiatives that keep rare diseases on the radar screen.  We promise to be available and engage in activities, especially as NORD moves forward with the FDA as they implement FDARA.

 

More on FDARA.....  

 


This website is an educational resource. It is not intended to provide medical advice or recommend a course of treatment. You should discuss all issues, ideas, suggestions, etc. with your clinician prior to use. Clinicians in a relevant field have reviewed the medical information; however, the Oley Foundation does not guarantee the accuracy of the information presented, and is not liable if information is incorrect or incomplete. If you have questions please contact Oley staff.

 

Updated in 2015 with a generous grant from Shire, Inc. 

 

This website was updated in 2015 with a generous grant from Shire, Inc. This website is an educational resource. It is not intended to provide medical advice or recommend a course of treatment. You should discuss all issues, ideas, suggestions, etc. with your clinician prior to use. Clinicians in a relevant field have reviewed the medical information; however, the Oley Foundation does not guarantee the accuracy of the information presented, and is not liable if information is incorrect or incomplete. If you have questions please contact Oley staff.
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