This OPEN ACT would make available to drug companies an "Orphan Product Exclusivity Extension" which would provide an additional six months of exclusivity to the patent life of the major market drug being repurposed for rare disease treatment.
This petition will be delivered to congress urging them to make simple legislative changes in support of rare diseases.
Join the Amyloidosis Foundation in support of this important legislation.
http://bit.ly/1BVsheE
The Binding Site: http://www.thebindingsite.com/al-amyloidosis
Australia: |
www.amyloidosis.com.au |
Brazil: |
www.paramiloidose.com.br |
Canada: |
www.thecasn.org |
Euramy: |
www.euramy.org |
France: |
www.cr.amylose-al.fr |
Italy: |
www.amiloidosi.it |
Germany: |
home.arcor.de/a-ludwig or www.amyloid.de |
The Netherlands: |
www.amyloid.nl |
Switzerland: |
www.amyloidose.ch |
United Kingdom: |
www.myeloma.org.uk |
Israel: |
israblog.nana10.co.il/blogread.asp?blog=530202 |
Israel Facebook: |
http://www.facebook.com/#!/groups/108804022537602 |
Portugal: |
www.paramiloidose.com |