+ + data and comments + +, page-5

I tend to add some references to the FDA, in case readers need it later on.

There are a number of key FDA sites and some are:

The FDA: US Food and Drug Administration
http://www.fda.gov/default.htm


Investigational New Drug (IND) Application Process:
http://www.fda.gov/cder/regulatory/applications/ind_page_1.htm


FAST TRACK, PRIORITY REVIEW AND ACCELERATED APPROVAL: http://www.accessdata.fda.gov/scripts/cder/onctools/Accel.cfm


Orphan Drug Designation.
http://www.fda.gov/orphan/designat/faq.htm


New FDA regulations to ensure supplement purity and quantity of ingredients:
http://www.ozestock.com.au/MessageView.asp?PostID=216092&Symbol=NRT


Gerry