|
IPCI IS THE BEST AND THE MOST UNDERVALUED UNKNOWN GEM IN THE BIOTECH SECTOR BUT PLEASE DO YOUR OWN RESEARCH ! GLTA
This Unknown ULTRA LOW FLOAT Stock awaiting 6 FDA approvals.IPCI has 15 Drugs in Pipeline many nearing ANDA/NDA filing including a potential...
Started by DollarChamp on
, 4 posts
by 2 people.
Answer Snippets (Read the full thread at OnlineTradersForum):
Are you recommending a buy? We....
If the release is not subject to a 30-month stay, the product could .
Intellipharmaceutics will not be subject to the automatic 30-month stay of FDA approval to market its approval by the FDA.
|
|
SAN FRANCISCO — A quarter-century after the U.S. Food and Drug Administration approved the first prescription drugs based on the main psychoactive ingredient in marijuana, additional medicines derived from or inspired by the cannabis plant itself could...
Started by by admin on
, 10 posts
by 8 people.
Answer Snippets (Read the full thread at denverpost):
Doesn't the FDA know that marijuana is a schedule 1 "drug" with NO KNOWN MEDICAL VALUE? Doesn't the FDA know that marijuana ....
Of other natural remedies which get shunned by the FDA and the governmnet lobbies in favor of much more.
|
|
This is a positive development for the shift in thinking about nutraceuticals being delivered as fda approved medicine.
Answer Snippets (Read the full thread at linkedin):
(link added) I personally think ny FDA approval should.
As it will several other industries.
|
Ask your Facebook Friends
|
Feeding off our Petition, " FDA Blocks Life-Saving Drug " ( Google it and please sign ! ), we at " Our Her2 Cancer Struggle " ( FB) are having a Rally. Tuesday, December 6th. 11:30 A.M. At the Flagpoles in front of Boston City Hall. Survivor Speakers ...
Started by phil on
, 15 posts
by 9 people.
Answer Snippets (Read the full thread at her2support):
But were persuaded....
Edited.
The real argument is with the FDA.
Wanted to close Expanded Access right after the FDA declined approval requires ALL data to be collated into their approval processes.
Some in the co.
Decision-making.
|
|
This is more of a legal thing then political...but we'll see. FYI this is about adult stem cells not embryonic stem cells...so save the baby-mama drama.
http://www.anh-usa.org/fda-new-claim-body-is-a-drug/
My favorite part of the whole thing is this comment...
Started by Senturon on
, 13 posts
by 3 people.
Answer Snippets (Read the full thread at fatwallet):
Http://www.anh-usa.org/fda-new would depress the market for out-of-state drugs that are approved by FDA." Ah, so because something or no better than conventional....
Adult stem cells not embryonic stem cells...so save the baby-mama drama .
|
|
Has anyone any insight into how long it takes FDA approved drugs to reach the shores of the UK, or other countries for that matter?
Obvoiusly I have the new drug in mind, and subsequently the next one ( 890?), Oh and on that note, fantastic news on the...
Started by User on
, 13 posts
by 1 people.
Answer Snippets (Read the full thread at cysticfibrosis):
If you do not have G551D and are hoping for approval for the drug for another mutation, i think?
As for how long it takes...often times the EU follows suit immediately after the FDA because it is possible.
|
|
On Sun, 14 Mar 2010 05:29:57 -0000, "Scott T" <sapsara@yahoo.com
Hello Group,
Do you think FDA will approve BMHR for uses in the US? Are there any doctors in the US who are using these devices? Is there anything wrong with designs? Why it is slow...
Started by Scott T on
, 4 posts
by 4 people.
Answer Snippets (Read the full thread at omgili):
Sapsara@yahoo.comSubject: [surfacehippy] BMHR and FDA approval
To: surfacehippy@yahoogroups.com
Date: Sunday, March 14 <markkenter@yahoo.com
Being that its is a Birmingham device, that Should help get approval one a surgeon ....
|
|
Now that it's through trials an FDA approved, does everyone with the G551D mutation go on it? For anyone who is on it or has a child on it, have you noticd any differences? My kids do not have the G551D mutation, they have DF508 and Q493X. When(if) VX...
Started by User on
, 6 posts
by 1 people.
Answer Snippets (Read the full thread at cysticfibrosis):
Ive been.
It was fast-tracked through FDA approval in just 3 months when it could have taken a year.
|
|
From what I understood they are not going to hire until approved. Many companies hire prior to FDA approval. I was told approval was not expected until March. Face 2 face would be the 2nd week in March. Anyone hear otherwise?
Answer Snippets (Read the full thread at cafepharma):
The goal here is to be respectfulIn the spirit....
The goal here to be a different company, we will issue offers contingent upon FDA approval.
Of trying to be a different company, we will issue offers contingent upon FDA approval.
|
|
January 3, 2012 - 3:35pm No news about EMEA approval here yet!
Hugs!
‹ The Sundance Book is NOW Finished! – “Let’s Talk About This…” Treating This Is As Good News but now looking at Thyroid
Answer Snippets (Read the full thread at cancer):
Articles/236730.php
Apparently is hasn't been approved, yet, by the FDA but it has been put on Orphan status that approval comes along soon!
yoga jo
January 3, 2012 - 7:40pm Was wondering, too, about very, very well in trials thus....
|
