U.S. Food and Drug Administration
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U.S. Food and Drug Administration | Facebook
facebook.com — “Welcome to the official Facebook Page about U.S. Food and Drug Administration. Join Facebook to start connecting with U.S. Food and Drug Administration.” View full resource at facebook.com
Most Recently Shared on September 29, 2010 at 8:53 pm By:
Good grief. Are any pharma employees going to be "Fans" of the FDA Facebook page? Sounds odd: http://www.facebook.com/FDA #hcsm
U.S. Food and Drug Administration | Facebook
facebook.com — “Welcome to the official Facebook Page about U.S. Food and Drug Administration. Join Facebook to start connecting with U.S. Food and Drug Administration.” View full resource at facebook.com
Most Recently Shared on October 7, 2010 at 7:48 pm By:
FDA's Favorite FB pages? White House, CDC, AIDS.gov and Healthcare.gov. http://ow.ly/2QeBN
U.S. Food and Drug Administration | Facebook
facebook.com — “Welcome to the official Facebook Page about U.S. Food and Drug Administration. Join Facebook to start connecting with U.S. Food and Drug Administration.” View full resource at facebook.com
Most Recently Shared on November 17, 2010 at 1:02 am By:
RT @iDailyScoop: #FDA on Fb http://on.fb.me/aagj05 Comment Policy" tab is glimpse of much needed pharma guidance policy #hcsmeu #hcsm
HHS Opens U.S. Food and Drug Administration Offices in India
hhs.gov — “HHS Secretary Mike Leavitt and Commissioner of the HHS Food and Drug Administration (FDA) Andrew C. von Eschenbach, M.D., today marked the opening of the HHS/FDA offices in New Delhi, and Mumbai, India.” View full resource at hhs.gov
Most Recently Shared on January 15, 2009 at 4:15 pm By:
HHS Opens FDA Offices in India http://www.hhs.gov/news/press/2009pres/01/20090115a.html
U.S. Food And Drug Administration Selects AB SCIEX To Provide Mass Spectrometry Systems For Food Contaminant Testing
medicalnewstoday.com — “AB SCIEX, a global leader in life science analytical technologies, announced that the U.S. Food and Drug Administration has purchased eight of the company's AB SCIEX QTRAP® 5500 Systems for an” View full resource at medicalnewstoday.com
Most Recently Shared on October 22, 2010 at 3:07 pm By:
U.S. Food And Drug Administration Selects AB SCIEX To Provide Mass Spectrometry Systems For Food Contaminant Testing http://mnt.to/3LBM
Incyte Submits New Drug Application for Ruxolitinib in Myelofibrosis to the US Food and Drug Administration
drugs.com — “Ruxolitinib is a new drug in development for the treatment of myelofibrosis. Ruxolitinib information includes news, clinical trial results and side effects.” View full resource at drugs.com
Most Recently Shared on June 10, 2011 at 2:02 am By:
Incyte Submits New Drug Application for Ruxolitinib in Myelofibrosis to the US Food and Drug Administratio... http://bit.ly/kCHd2A #drug
U.S. Food And Drug Administration Keeps Rosiglitazone (Avandia) On The Market With Restrictions
medicalnewstoday.com — “The U.S. Food and Drug Administration (FDA) has announced that it will significantly restrict the use of the diabetes drug rosiglitazone (brand name, Avandia) to patients with Type 2 diabetes who” View full resource at medicalnewstoday.com
Most Recently Shared on September 25, 2010 at 12:05 am By:
U.S. Food And Drug Administration Keeps Rosiglitazone (Avandia) On The Market With Restrictions http://mnt.to/3Kjr #diabetes
U.S. Food And Drug Administration Approves ABILIFY® (aripiprazole) For The Treatment Of Irritability Associated With Autistic Disorder In Patients
medicalnewstoday.com — “(BUSINESS WIRE)--Bristol-Myers Squibb Company (NYSE: BMY) and Otsuka Pharmaceutical Co., Ltd. announced that the U.S. Food and Drug Administration (FDA) has approved the supplemental New Drug Appl” View full resource at medicalnewstoday.com
Most Recently Shared on November 28, 2009 at 11:28 am By:
U.S. Food And Drug Administration Approves ABILIFY® (aripiprazole) For The Treatment Of Irritability Associated.. http://bit.ly/51H21G
U.S. Food And Drug Administration (FDA) Clears Novel ImageSenseTM Technology For Use With Colposcopy
medicalnewstoday.com — “STI Medical Systems, an industry leader in medical imaging systems and machine vision software, announced that the U.S. Food and Drug Administration (FDA) has given clearance to the Company's prec” View full resource at medicalnewstoday.com
Most Recently Shared on January 9, 2011 at 11:10 am By:
U.S. Food And Drug Administration (FDA) Clears Novel ImageSenseTM Technology For Use With Colposcopy:... http://mnt.to/f/3PMp #MedDevice
ZOLL Propaq M Monitor Granted 510(k) Clearance By U.S. Food And Drug Administration
medicalnewstoday.com — “ZOLL Medical Corporation (NasdaqGS: ZOLL), a manufacturer of medical devices and related software solutions, announced that it has received 510(k) clearance from the U.S. Food and Drug Administrat” View full resource at medicalnewstoday.com
Most Recently Shared on September 23, 2010 at 1:34 pm By:
ZOLL Propaq M Monitor Granted 510(k) Clearance By U.S. Food And Drug Administration: ZOLL Medical Corpor... http://mnt.to/f/3Kcm #MedDevice
U.S. Food and Drug Administration Approves Crestor for Use in Pediatric Patients With Heterozygous Familial Hypercholesterolemia
drugs.com — “Crestor (rosuvastatin calcium) is used to treat pediatric patients with heterozygous familial hypercholesterolemia. Includes Crestor side effects, interactions and indications.” View full resource at drugs.com
Most Recently Shared on October 16, 2009 at 10:03 pm By:
FDA Approves Crestor for Use in Pediatric Patients With Heterozygous Familial Hypercholesterolemia - http://bit.ly/DrHi0
Auxilium Announces U.S. Food and Drug Administration Approval for Xiaflex for the Treatment of Dupuytren's Contracture
drugs.com — “Xiaflex (collagenase clostridium histolyticum) is used to treat Dupuytren's contracture. Includes Xiaflex side effects, interactions and indications.” View full resource at drugs.com
Most Recently Shared on February 3, 2010 at 10:07 pm By:
Auxilium Announces FDA Approval for Xiaflex for the Treatment of Dupuytren's Contracture - http://bit.ly/cV10Uc
Depomed Announces US Food and Drug Administration Approval of Gralise (gabapentin) Once-Daily Tablets for Treatment of Post-Herpetic Neuralgia
drugs.com — “Gralise (gabapentin) is used to treat post-herpetic neuralgia. Includes Gralise side effects, interactions and indications.” View full resource at drugs.com
Most Recently Shared on February 1, 2011 at 11:10 pm By:
Depomed Announces US Food and Drug Administration Approval of Gralise (gabapentin) Once-Daily Tablets for ... http://bit.ly/eeb147 #drug
Depomed Announces US Food and Drug Administration Approval of Gralise (gabapentin) Once-Daily Tablets for Treatment of Post-Herpetic Neuralgia
drugs.com — “Gralise (gabapentin) is used to treat post-herpetic neuralgia. Includes Gralise side effects, interactions and indications.” View full resource at drugs.com
Most Recently Shared on February 3, 2011 at 12:16 am By:
Depomed Announces FDA Approval of Gralise (gabapentin) for Treatment of Post-Herpetic Neuralgia - http://bit.ly/hLaEa7
U.S. Food And Drug Administration Keeps Rosiglitazone (Avandia) On The Market With Restrictions - QualityPoint Technologies
qualitypointtech.net — “The U.S. Food and Drug Administration (FDA) has announced that it will significantly restrict the use of the diabetes drug rosiglitazone (brand name, Avandia) to patients with Type 2 diabetes who cannot control their diabetes on other medications. Their decision is in response to data that suggest an increased risk of cardiovascular events, such as heart attack and stroke, in patients who were treated with rosiglitazone...” View full resource at qualitypointtech.net
Most Recently Shared on September 25, 2010 at 9:00 am By:
U.S. Food And Drug Administration Keeps Rosiglitazone (Avandia) On The Market With Restrictions: The U.S. Food and... http://bit.ly/bgbNfQ
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Jonathan Richman
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