training

Anonymous

Guest
Does anyone know what our training timeline is like? When I interviewed the first round - I didnt get a clear pciture. I know we don't have our final letter until after approval this week and the start date is 1-17-11. However, anything after that I am not sure about. Thanks for replies.

Excited to get started.
 










































KV is done put a fork in it

ST. LOUIS, Jan. 12, 2011 /PRNewswire/ -- K-V Pharmaceutical Company (NYSE: KVa/KVb) today issued an update on the status of the U.S. Food and Drug Administration's review of Hologic, Inc.'s (Hologic) New Drug Application (NDA) for Gestiva™ (hydroxyprogesterone caproate injection) as a treatment for the prevention of preterm birth in women with a singleton pregnancy who have a history of singleton spontaneous preterm birth.

Following the July 2010 resubmission of the NDA by Hologic, the FDA assigned a Prescription Drug User Fee Act ("PDUFA") action date of January 13, 2011. Hologic advised the Company that the FDA had recently requested additional information with respect to the Gestiva™ application. The requested information was provided to the FDA on January 10, 2011.

In order to provide for additional time to review the information that was solicited by the FDA and provided by Hologic, the FDA has extended the PDUFA date to April 13, 2011. Based on the information provided, the Company remains confident in the approval of Gestiva™ and believes a positive action by the FDA is likely on or before the new PDUFA date.

In light of this new information, the Company further stated that it is evaluating its liquidity outlook. When the Company completes its evaluation, it intends to furnish an update as appropriate.

About Preterm Birth

According to the March of Dimes, preterm birth, or the birth of a baby prior to 37 completed weeks of pregnancy, affects one in eight babies born in the United States. Preterm birth is the leading cause for infant mortality and morbidity. Babies born preterm tend to grow more slowly, have more problems with their eyes, ears, breathing and nervous system, and experience more learning and behavioral problems. Preterm birth has been estimated to cost the United States more than $26 billion a year.

About K-V Pharmaceutical Company
K-V Pharmaceutical Company is a fully-integrated specialty pharmaceutical company that develops, manufactures, markets, and acquires technology-distinguished branded prescription pharmaceutical products. The company markets its technology-distinguished products through Ther-Rx Corporation, its branded drug subsidiary.
 












Seriously.... does this mean they are not getting approval tomorrow??

How stupid can you be? Read the press release.

FDA 'could' act before April 13, but won't, because they don't have to. Still could ask for more information, hand down an 'approvable' (which means more data, trials, etc), approve it, or NOT approve it. They can and will do whatever they want.
 






Its a 90 day review which means they need to give the fda more information. Doesn't look good considering they had two years to get the fda all the information needed from the previous rejection. Time to keep looking for another job this place doesn't look like they will make it.
 












I just hope they get the approval despite all that the media and reports I am reading say. This drug can help so many. I havent heard anything from quintiles so I am going to assume they are waiting until tomorrow to share any news with us.