Generic drugmakers submitting abbreviated new drug applications (ANDAs) and prior approval supplements (PAS) will see their US Food and Drug Administration (FDA) fee rates drop in 2017, though all other rates, including those for drug master files (DMF) and facility fees will increase when compared to 2016. 481 more words
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Today’s First Draft Friday entry is short and sweet and focused on my battle with the Spec Script.
Writing a spec script is WEIRD.
You take someone else’s characters and voice and you mesh yours into the middle of it, but only so much so that you don’t disrupt the overall tone or change the characters too terribly much. 1,395 more words
I’ve been giving a lot of thought about what I want this blog to be.
Mostly, I want to talk about books.
But, I’m a writer too, and part of being a writer is finding ways to put your own work out there, in all of its forms and with all of its flaws, so starting this Friday, I’ll be doing “First Draft Friday”, where I’ll post a small piece of unpolished first draft quality writing. 283 more words