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i am going to an interview with PDI on tuesday- anyone interviewing with Braeburn? Have they named the 4 DM's yet? if so any word on what pharma company they came from?
 






Anyone who goes into that PDI contract will have to have addiction medicine experience, like a displaced Reckitt rep or someone who worked for Alkermes with Vivitrol. If you don't know addiction medicine, you can't just walk in and try to sell them. All of the addiction practitioners, whether addiction medicine or addiction psychiatrists, know each other and they communicate a lot. One bad detail will get around quick. One bad detail and you'll lose all credibility. It's not an area where you can wing it, because the prescribers will nail you on the spot.
 






Anonymous said:
Anyone who goes into that PDI contract will have to have addiction medicine experience, like a displaced Reckitt rep or someone who worked for Alkermes with Vivitrol. If you don't know addiction medicine, you can't just walk in and try to sell them. All of the addiction practitioners, whether addiction medicine or addiction psychiatrists, know each other and they communicate a lot. One bad detail will get around quick. One bad detail and you'll lose all credibility. It's not an area where you can wing it, because the prescribers will nail you on the spot.
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LOL "one bad detail....." BS
 












Anonymous said:
Anyone who goes into that PDI contract will have to have addiction medicine experience, like a displaced Reckitt rep or someone who worked for Alkermes with Vivitrol. If you don't know addiction medicine, you can't just walk in and try to sell them. All of the addiction practitioners, whether addiction medicine or addiction psychiatrists, know each other and they communicate a lot. One bad detail will get around quick. One bad detail and you'll lose all credibility. It's not an area where you can wing it, because the prescribers will nail you on the spot.
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How about one bad J code you twit!
 












Just got a call from PDI about this position. Any word on what the base pay is? Company car? Vacation? Seems my PDI rep did not know many of the questions I was asking. Serious answers would be great!
 






Anonymous said:
Just got a call from PDI about this position. Any word on what the base pay is? Company car? Vacation? Seems my PDI rep did not know many of the questions I was asking. Serious answers would be great!
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base 80s. car allowance. i don't know how your PDI recruiter didn't have the answers to these questions...it seems like those are the ONLY answers they have!
 






















































Reading all of the investment boards, it looks like Braeburn or Titan will have to ante up some bucks and a lot of time for the data FDA wants.

I'm sure to the FDA advisory committee it sure sounded like a good idea, but when you dig into the data the product didn't do that well in clinical trials. Even if it is approved, it will be a dog.
 






Anonymous said:
Reading all of the investment boards, it looks like Braeburn or Titan will have to ante up some bucks and a lot of time for the data FDA wants.

I'm sure to the FDA advisory committee it sure sounded like a good idea, but when you dig into the data the product didn't do that well in clinical trials. Even if it is approved, it will be a dog.
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Another idiot. Probuphine is the same active drug as buprenorphine. The drug works, the question pertained to what would be an adequate dose. You really read "all" of the boards?
 






Anonymous said:
Another idiot. Probuphine is the same active drug as buprenorphine. The drug works, the question pertained to what would be an adequate dose. You really read "all" of the boards?
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You didn't read the investor boards, did you, moron? Titan has about $13 million in cash, and Braeburn has to make the decision whether to fund the additional trials or not. The clinical trial results did not establish an equivalent dose for Suboxone/Subutex and the daily dose of buprenorphine received may serve as an agonist but not an antagonist. You don't know much about the drug, halfwit. FDA's concerns were also with the required REMS program. The surgical procedure to remove or insert the rods was also questioned for possible adverse events just like those seen with Norplant while it was still on the market.

And yes, I did read ALL of the available boards. Most of them were duplicates, so if you read even the first ten entries on Google, you would know that.

Next time try actually doing some background research before you shoot off your ignorant mouth. Either this product is dead in the water or it will take more time and money than Braeburn or Titan might be willing to spend.
 






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