Deleted Tweets From Scott Gottlieb, R-D.C.

Deleted Tweets From Scott Gottlieb, R-D.C.

Scott Gottlieb's accounts: SGottliebFDA

Tracking Since: October 20, 2017

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About 3 out of 4 teens smokers will become adult smokers. We’re going to be taking new steps in 2018 to address adolescent and teen use of tobacco products https://t.co/o48I8OqGof https://t.co/FoazgXzycS

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#FDA’s record number of novel 2017 approvals of drug and biologics (56); devices (95); and generics (1,027) was culmination of years of dedicated efforts by staff to modernize policies; a wave of scientific progress; and new legislation like Cures Act tha

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March 19 FDA workshop on Patient-Focused Drug Development: Developing and Submitting Proposed Draft Guidance Relating to Patient Experience Data https://t.co/gBffnNCrL6#PFDD

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3/3 Americans MUST have confidence FDA acts quickly in setting of food recalls to protect them. This is the core of our consumer protection role. We’ve improved much; will prove it with updated data; and will make process even better in 2018. Wish everyon

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2/3 We made MANY processs improvements to speed food recalls; increase our rigor. We’ll release updated analysis - from 2017 NOT 2012 - on how we’re doing. More reforms in store for 2018; including changes to make sure we release much more info to consume

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1/2 This report, first released in 2016, was re-released over Christmas. It’s based on a selective review of 30 complex food recalls from 2012-2015 out of 1,000s performed. In many of the 30 FDA was slow to act. Even a few flawed recalls are too many. We

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#FDA is working closely with industry and local and federal officials to address the shortage situation for IV saline as a result of #HurricaneMaria. We expect the shortage of IV fluids will improve in early 2018 based on information we’re receiving from

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FDA believes strongly people addicted to opioids should have access to safe and effective treatments for addiction.  Unfortunately, unscrupulous vendors are trying to capitalize on the opioid epidemic by illegally marketing products for these purposes htt

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#FDA’s new Predictive Toxicology Roadmap and novel methods for toxicity testing will help us move safe products to market more efficiently; reduce reliance on animal testing for tox https://t.co/xOrLiU3vRJ

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#FDA must encourage the development of tools that can help people be more informed about their health. We know our regulations play a crucial role in the innovation of #digitalhealth; 4 guidances released today provide greater clarity on our role https://

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RT @SGottliebFDA: #FDA outlines a new approach to the development of drugs for a rare pediatric disease that could reduce the need fo… https://t.co/MyIHqRMwC7

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RT @SGottliebFDA: #FDA’s public health mandate; gravity of opioid crisis compel us to take new steps to encourage more widespread inn… https://t.co/XiBVJXtoOt

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#FDA taking new steps to promote innovation in products that can help smokers quit combustible cigarettes as part o… https://t.co/wsvREjfHly

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#FDA began patent submission date data collection in 2013. There are now about 4,000 patent records for which submi… https://t.co/EGSP27iZFA

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My statement on new steps #FDA is taking today to promote development of generic versions of opioids formulated to… https://t.co/bEDmF5WA7i

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RT @NYTHealth: The F.D.A. speeds review of some gene, cell therapies, a move desired by the industry. Critics want more oversight. https://t.co/qVlNGGB5u0

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(3/3) As commissioner, I’m personally committed to this effort. It’s one of my highest priorities. In collaboration… https://t.co/4Gb3YksCDO

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Reason Magazine: The #FDA Will Finally Let You See Your Genetic Information https://t.co/DICx5hTM6M

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