12.29 The FDA: US Food and Drug Administration http://www.fda.gov/default.htm
12.29.1 Investigational New Drug (IND) Application Process: http://www.fda.gov/cder/regulatory/applications/ind_page_1.htm
12.29.2 FAST TRACK, PRIORITY REVIEW AND ACCELERATED APPROVAL: http://www.accessdata.fda.gov/scripts/cder/onctools/Accel.cfm
12.29.3 Orphan Drug Designation. http://www.fda.gov/orphan/designat/faq.htm
12.29.4 New FDA regulations to ensure supplement purity and quantity of ingredients: http://www.ozestock.com.au/MessageView.asp?PostID=216092&Symbol=NRT
Gerry
EIF Price at posting:
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