Replies to post #207124 on Anavex Life Sciences Corp (AVXL)

[nidan7500]

I would like to see the FDA change it's thinking from..."First, do no harm" to "first, do it right, then get it done".
We all know the FDA does exceptional process control and documentation and associated rule setting, but they need to figure out how to gate the process better and in a more timely manner. BTW, what do we pay the NIH to do?

[Investor2014]

The company then submits an application (usually about 100,000 pages) to the FDA for approval

I can't begin to imagine what to write on 100,000 pages that you can be guaranteed no one will read.

Maybe just repeat:

The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
The FDA is slow and stupid
and so on....please approve when finished reading.