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Soon... In 4 months
admin
yellow stickie 11745 on all boards
Don't fall in love with a stock
Don't Pledge your allegiance to a stock
Correct, the PRs said nothing until 120 days. Come back in April, hold thru June and you'll make money, show is over here.
Selling because nothing going on here until 60 - 120 days from now.
This will drop to 3, then start moving up in 60 days....that's 2 months from now. No reason to be here until then. Make money elsewhere, come back later.
Article of no substance
Why was it released?
Re: news today
Another reason Dr Rubinfeld signed on full time rather than be an advisor.
What about baby squirrels
sold all, I'm out
back in a month or two
Big pharma eyebrows are raised
Agreed, good science ongoing, developments rapidly coming to surface. Helps overall development of cancer therapy.
In an effort to ensure that patients in the U.S. have access to high-quality, safe and effective medical devices, the medical device clinical trials program at the FDA has undergone many changes. Some of these changes include issuing guidance documents and revising organizational structure and policies. Although we’ve communicated these changes individually, this event will provide you an opportunity to hear about the current medical device clinical trials program, outlining where we are now and where we are going.
On January 22, 2014 from 1:30 PM – 3:00 PM, Eastern Time, the FDA will hold a webinar to provide an overview of the Medical Device Clinical Trials Program. Participants will also have an opportunity to ask questions.
Topics to be covered during the webinar:
Clinical Trial Strategic Priority
IDE SOP Implementation
FY14 Performance and FY15 Performance Goals
Early Feasibility Studies
Future Program Plans
Webinar Details:
Date: January 22, 2014
Time: 1:30 PM – 3:00 PM, Eastern Time
To ensure you are connected, log-in by 1:15 PM.
To hear the presentation and ask questions:
Dial: 800-369-1937; passcode: 5211887
International: 1-312-470-7075; passcode: 5211887
To view the slide presentation during the webinar:
https://www.mymeetings.com/nc/join.php?i=PW1052941&p=5211887&t=c
Following the webinar, a transcript, recording and slides will be available at: http://www.fda.gov/CDRHWebinar
Please Note: the slide presentation will also be available at this site on the morning of the webinar.
If you have any questions about the webinar, please contact CDRH Learn.
To view past webinars on clinical trials and other topics, please visit: www.fda.gov/CDRHWebinar
Food and Drug Administration
Center for Devices and Radiological Health
EOD Buying time
FDA Webinar
In an effort to ensure that patients in the U.S. have access to high-quality, safe and effective medical devices, the medical device clinical trials program at the FDA has undergone many changes. Some of these changes include issuing guidance documents and revising organizational structure and policies. Although we’ve communicated these changes individually, this event will provide you an opportunity to hear about the current medical device clinical trials program, outlining where we are now and where we are going.
On January 22, 2014 from 1:30 PM – 3:00 PM, Eastern Time, the FDA will hold a webinar to provide an overview of the Medical Device Clinical Trials Program. Participants will also have an opportunity to ask questions.
Topics to be covered during the webinar:
Clinical Trial Strategic Priority
IDE SOP Implementation
FY14 Performance and FY15 Performance Goals
Early Feasibility Studies
Future Program Plans
Webinar Details:
Date: January 22, 2014
Time: 1:30 PM – 3:00 PM, Eastern Time
To ensure you are connected, log-in by 1:15 PM.
To hear the presentation and ask questions:
Dial: 800-369-1937; passcode: 5211887
International: 1-312-470-7075; passcode: 5211887
To view the slide presentation during the webinar:
https://www.mymeetings.com/nc/join.php?i=PW1052941&p=5211887&t=c
Following the webinar, a transcript, recording and slides will be available at: http://www.fda.gov/CDRHWebinar
Please Note: the slide presentation will also be available at this site on the morning of the webinar.
If you have any questions about the webinar, please contact CDRH Learn.
To view past webinars on clinical trials and other topics, please visit: www.fda.gov/CDRHWebinar
Food and Drug Administration
Center for Devices and Radiological Health
FDA
In an effort to ensure that patients in the U.S. have access to high-quality, safe and effective medical devices, the medical device clinical trials program at the FDA has undergone many changes. Some of these changes include issuing guidance documents and revising organizational structure and policies. Although we’ve communicated these changes individually, this event will provide you an opportunity to hear about the current medical device clinical trials program, outlining where we are now and where we are going.
On January 22, 2014 from 1:30 PM – 3:00 PM, Eastern Time, the FDA will hold a webinar to provide an overview of the Medical Device Clinical Trials Program. Participants will also have an opportunity to ask questions.
Topics to be covered during the webinar:
Clinical Trial Strategic Priority
IDE SOP Implementation
FY14 Performance and FY15 Performance Goals
Early Feasibility Studies
Future Program Plans
Webinar Details:
Date: January 22, 2014
Time: 1:30 PM – 3:00 PM, Eastern Time
To ensure you are connected, log-in by 1:15 PM.
To hear the presentation and ask questions:
Dial: 800-369-1937; passcode: 5211887
International: 1-312-470-7075; passcode: 5211887
To view the slide presentation during the webinar:
https://www.mymeetings.com/nc/join.php?i=PW1052941&p=5211887&t=c
Following the webinar, a transcript, recording and slides will be available at: http://www.fda.gov/CDRHWebinar
Please Note: the slide presentation will also be available at this site on the morning of the webinar.
If you have any questions about the webinar, please contact CDRH Learn.
To view past webinars on clinical trials and other topics, please visit: www.fda.gov/CDRHWebinar
Food and Drug Administration
Center for Devices and Radiological Health
but not that news...
FDA News
Webinar
In an effort to ensure that patients in the U.S. have access to high-quality, safe and effective medical devices, the medical device clinical trials program at the FDA has undergone many changes. Some of these changes include issuing guidance documents and revising organizational structure and policies. Although we’ve communicated these changes individually, this event will provide you an opportunity to hear about the current medical device clinical trials program, outlining where we are now and where we are going.
On January 22, 2014 from 1:30 PM – 3:00 PM, Eastern Time, the FDA will hold a webinar to provide an overview of the Medical Device Clinical Trials Program. Participants will also have an opportunity to ask questions.
Topics to be covered during the webinar:
Clinical Trial Strategic Priority
IDE SOP Implementation
FY14 Performance and FY15 Performance Goals
Early Feasibility Studies
Future Program Plans
Webinar Details:
Date: January 22, 2014
Time: 1:30 PM – 3:00 PM, Eastern Time
To ensure you are connected, log-in by 1:15 PM.
To hear the presentation and ask questions:
Dial: 800-369-1937; passcode: 5211887
International: 1-312-470-7075; passcode: 5211887
To view the slide presentation during the webinar:
https://www.mymeetings.com/nc/join.php?i=PW1052941&p=5211887&t=c
Following the webinar, a transcript, recording and slides will be available at: http://www.fda.gov/CDRHWebinar
Please Note: the slide presentation will also be available at this site on the morning of the webinar.
If you have any questions about the webinar, please contact CDRH Learn.
To view past webinars on clinical trials and other topics, please visit: www.fda.gov/CDRHWebinar
Food and Drug Administration
Center for Devices and Radiological Health
Usually insiders sell during Dec for tax reasons. Buying on the de Novo news is an indication that FDA change of class will be approved, just a matter of waiting through FDA bureaucracy.
Same with the phone. New Iphone six is thinner, made from aluminum, but since it has shown to bend, it may be the future design and mold to be used with LM, as soon as machinery and facility is up, guesssing next version. Can't have bendable phones out there longer than 1 version.
Sometimes patent continuations are filed as a preclude to getting biz in order before a JV or buyout. Sometimes
true, just going out to swing some at the golf club
same here, out for today, expecting dip midweek, back to 9 fri
Some sell because 4th qtr report won't come out until mid Feb, same with FDA news. There's time to come back in lower.
All around the time of the de novo filing, which indcates they've been in touch with the FDA and this is a done deal.
Why does ticker above say green 7% when it was zero gain?
that's intercept pharmaceuticals
Buy big to end the year
if we all mailed in $20 to the company, would they show it as revenue?
Today's news is why Rubenfeld signed on.
Adding more to my pile tomorrow. This will go toward my xmas Ducati I'll give as a present to myself.
It's starting...
FDA is re-inking approval stamp pad. After the fourth coffee break, boom
Why does the ticker say 15% Increase when Schwab says zero increase for the day.
PR and SA article after EOD?
The SA article is waiting at the starting gate snorting like Secretariat
If an article is based on a project event they are very dependable. If article is based on conjecture and forecasts, they are good, but sometimes off.
Since this article Was based on an upcoming probably, it seems like the timing was off. Look for eminent probably soon.