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

We’re evaluating the comments we received and will advance a new approach to how we treat maple syrup and honey under the new nutrition facts label. We’ve heard the concerns, and we’re developing new guidance to address those challenges https://t.co/OfsT2

FDA and CMS data presented at today’s #ACIP looked at large pool of real world data from more than 13 million beneficiaries 65 & older. Cell-cultured (10.4% >) and high dose vaccines (8.4>) were both marginally more effective than egg-based quad

#FDA is committed to working with stakeholders as we continue to evaluate VE among different types of VE not only for the 2017-18 season, but for future seasons.

First of four planned FDA draft guidances on Patient-Focused Drug Development: Collecting Comprehensive and Representative Input #PFDD https://t.co/cBN5GUi7jr https://t.co/UHFjWXaHDJ

RT @FDATobacco: FDA is seeking information related to the role that flavors, including menthol, play in tobacco products. Share y… https://t.co/aUOTBHT84U

We have advised Perrigo that it failed to comply with #FDA postmarketing requirements for a study intended to determine the cardiovascular effects of testosterone replacement therapy product, Testosterone Gel, by the agreed upon deadline. https://t.co/DVS

Postmarketing studies are important, providing additional evaluation after a drug is approved. A company is responsible for adhering to the timetable for completing postmarketing studies, and we are prepared to take action when companies fail to comply.

RT @FDAOncology: Focusing on Core Patient-Reported Outcomes in Cancer Clinical Trials: Symptomatic Adverse Events, Physical Function… https://t.co/DRRTjiHkgF

#FDA remains committed to making sure industry fulfills their PMRs in a timely manner and that studies are transparent to the public. Overall, the majority of PMRs and PMCs are progressing toward completion according to the agreed-upon schedule. https://t

RT @FDAOncology: Incorporating the #patientexperience into regulatory decision making in the USA, Europe, and Canada… https://t.co/LMrzwh7sf0

RT @GeorgiaGrown: Thank you to @SGottliebFDA for recognizing the efforts of NASDA towards implementing FSMA in a judicious and responsible… QT @SGottliebFDA: I want to thank the leadership of @NASDAnews for visiting with me and my team at #FDA today. Our partnership with N… https://t.co/0oP8Ly47Az)

RT @FDAcdrhIndustry: First continuous glucose monitoring system that includes a fully implantable glucose sensor that can be worn up to… https://t.co/ZNYvvoWvsg

RT @RAPSorg: .@US_FDA's CBER Launches new Program for Early Interaction With Biologics Developers | #Regulatory Focus… https://t.co/NnaSI8btbc

RT @FDAanimalhealth: Would you like a career at CVM? Be sure to check our vacancy announcements here: https://t.co/KRilfN2osm #CVMCareers#CVMCarreras

The US has one of the safest food supplies in the world. #FDA continues to make sure the abundant, diverse, and complex global food supply is safe, and that food imported into the US is held to the same standards as food produced at home https://t.co/Tc09

RT @SGottliebFDA: 1/6 #FDA is committed to helping foster development and approval of innovative medical products. Today’s launch of… https://t.co/2b43zbZIQr

RT @PatrickConwayMD: I am honored to be on MH Top 50 physician executives list with friends and colleagues, https://t.co/auqgPvds4P. Too m… QT @modrnhealthcr: Patrick Conway, CEO of Blue Cross and Blue Shield of North Carolina, is #23. Check out who else made this year's li… https://t.co/lv6HDjqAxS)

SUNDAY TWEETORIAL: For those who follow me, you’ll know that the topic of this week’s #FDA Sunday Tweetorial is among the most critical: food safety. FDA takes our responsibility for assuring safety of the food supply seriously, and food safety is one of

RT @BiotechSusan: FDA Commissioner @SGottliebFDA elaborates on his proposal for fixing the broken #antibiotics business model, via… https://t.co/8O5l8dqRHN

FDA collaborates closely with CDC on WGS, as CDC has sequencing capacity across the US to perform WGS on pathogens from ill people, while #FDA conducts sequencing on pathogens identified in foods and settings like food manufacturing plants https://t.co/jY

We’re evaluating the comments we received and will advance a new approach to how we treat maple syrup and honey under the new nutrition facts label. We’ve heard the concerns, and we’re developing new guidance to address those challenges https://t.co/OfsT2

FDA and CMS data presented at today’s #ACIP looked at large pool of real world data from more than 13 million beneficiaries 65 & older. Cell-cultured (10.4% >) and high dose vaccines (8.4>) were both marginally more effective than egg-based quad

#FDA is committed to working with stakeholders as we continue to evaluate VE among different types of VE not only for the 2017-18 season, but for future seasons.

First of four planned FDA draft guidances on Patient-Focused Drug Development: Collecting Comprehensive and Representative Input #PFDD https://t.co/cBN5GUi7jr https://t.co/UHFjWXaHDJ

RT @FDATobacco: FDA is seeking information related to the role that flavors, including menthol, play in tobacco products. Share y… https://t.co/aUOTBHT84U

We have advised Perrigo that it failed to comply with #FDA postmarketing requirements for a study intended to determine the cardiovascular effects of testosterone replacement therapy product, Testosterone Gel, by the agreed upon deadline. https://t.co/DVS

Postmarketing studies are important, providing additional evaluation after a drug is approved. A company is responsible for adhering to the timetable for completing postmarketing studies, and we are prepared to take action when companies fail to comply.

RT @FDAOncology: Focusing on Core Patient-Reported Outcomes in Cancer Clinical Trials: Symptomatic Adverse Events, Physical Function… https://t.co/DRRTjiHkgF

#FDA remains committed to making sure industry fulfills their PMRs in a timely manner and that studies are transparent to the public. Overall, the majority of PMRs and PMCs are progressing toward completion according to the agreed-upon schedule. https://t

RT @FDAOncology: Incorporating the #patientexperience into regulatory decision making in the USA, Europe, and Canada… https://t.co/LMrzwh7sf0

RT @GeorgiaGrown: Thank you to @SGottliebFDA for recognizing the efforts of NASDA towards implementing FSMA in a judicious and responsible… QT @SGottliebFDA: I want to thank the leadership of @NASDAnews for visiting with me and my team at #FDA today. Our partnership with N… https://t.co/0oP8Ly47Az)

RT @FDAcdrhIndustry: First continuous glucose monitoring system that includes a fully implantable glucose sensor that can be worn up to… https://t.co/ZNYvvoWvsg

RT @RAPSorg: .@US_FDA's CBER Launches new Program for Early Interaction With Biologics Developers | #Regulatory Focus… https://t.co/NnaSI8btbc

RT @FDAanimalhealth: Would you like a career at CVM? Be sure to check our vacancy announcements here: https://t.co/KRilfN2osm #CVMCareers#CVMCarreras

The US has one of the safest food supplies in the world. #FDA continues to make sure the abundant, diverse, and complex global food supply is safe, and that food imported into the US is held to the same standards as food produced at home https://t.co/Tc09

RT @SGottliebFDA: 1/6 #FDA is committed to helping foster development and approval of innovative medical products. Today’s launch of… https://t.co/2b43zbZIQr

RT @PatrickConwayMD: I am honored to be on MH Top 50 physician executives list with friends and colleagues, https://t.co/auqgPvds4P. Too m… QT @modrnhealthcr: Patrick Conway, CEO of Blue Cross and Blue Shield of North Carolina, is #23. Check out who else made this year's li… https://t.co/lv6HDjqAxS)

SUNDAY TWEETORIAL: For those who follow me, you’ll know that the topic of this week’s #FDA Sunday Tweetorial is among the most critical: food safety. FDA takes our responsibility for assuring safety of the food supply seriously, and food safety is one of

RT @BiotechSusan: FDA Commissioner @SGottliebFDA elaborates on his proposal for fixing the broken #antibiotics business model, via… https://t.co/8O5l8dqRHN

FDA collaborates closely with CDC on WGS, as CDC has sequencing capacity across the US to perform WGS on pathogens from ill people, while #FDA conducts sequencing on pathogens identified in foods and settings like food manufacturing plants https://t.co/jY