FDA keeps opening dockets and collecting comments and refusing to 
follow its laws and order safety trials.  Here's another:

"FDA is opening this docket to permit individuals other than 
manufacturers to submit information related to the safety and 
effectiveness of ECT."

Comment here:

<http://www.regulations.gov/search/Regs/home.html#submitComment?R=0900006480a20202>http://www.regulations.gov/search/Regs/home.html#submitComment?R=0900006480a20202 


Even though I selected 'individual consumer', the online form seems 
to require an organization.  You may choose your own, or use People 
Who or CTIP.

Here's what I said: I consider ECT high-risk and believe it should 
remain Class III until real testing shows otherwise.

Sylvia


www.peoplewho.org