FDA Public Hearing on Antiseptic Patient Preoperative Skin Preparation Products

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Updated October 12, 2022

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You can still read about the same topic here:

Safety and Effectiveness for Health Care Antiseptics; TopicalAntimicrobial Drug Products for Over-the-Counter HumanUse; Proposed Amendment of the Tentative Final Monograph;Reopening of Administrative Record - FDA.gov (PDF)  

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News & Events > Antiseptic Patient Preoperative Skin Preparation Products:

"The Food and Drug Administration (FDA or the Agency) is announcing a public hearing to obtain input on how to address microbial contamination of patient preoperative skin preparation drug products. Currently, patient preoperative skin preparations are not required to be sterile, and bacteria can contaminate these products at the time of manufacture or during product use. Contaminated patient preoperative skin preparations have been associated with clinical infections and adverse outcomes. At this public hearing, FDA is interested in obtaining public comment about certain scientific and product use issues related to patient preoperative skin preparations"

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Meeting Details:

Date(s):      December 12 - 13, 2012

Time:           9:00 a.m. to 4:00 p.m.

Location:     DoubleTree by Hilton Hotel Washington DC/Silver Spring
                      The Ballrooms
                      8727 Colesville Road
                      Silver Spring, MD 20910

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What You Should Know for the upcoming Flu Season - from the CDC

Updated May 7, 2019

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You might also be interested in:
Influenza (Flu) - CDC:  Learn about the current flu season & treatments, and more!


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Follow the link below to checkout the CDC's very comprehensive Q & A webpage. Lots of answers to just about every question you might ask.

CDC - Seasonal Influenza (Flu) - What You Should Know for the 2012-2013 Influenza Season:
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FDA Increases Winery Inspections

FDA Takes a Growing Interest in Winery Safety | News | News & Features | Wine Spectator:

"While winery inspections are not new, they’re being ramped up under the 2011 Food Safety Modernization Act, according to FDA spokeswoman Patricia El-Hinnawy.

The federal law mandates that the FDA inspect all food processing establishments. The frequency of inspections is based on safety risk and compliance history. While wineries are considered low risk because the fermentation process kills pathogens, all food facilities must be inspected within seven years and at least once every five years after that. “The FDA may be conducting more inspections [at wineries] than it has done in the recent past, in order to meet the [law’s] requirements,” El-Hinnawy said."

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FDA on the Ranbaxy Atorvastatin Recall

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The FDA is providing additional related information. Just follow the link below.

Drug Safety and Availability > FDA Statement on the Ranbaxy Atorvastatin Recall:

"FDA Statement on the Ranbaxy Atorvastatin Recall

Update: 11/30/2012
FDA is notifying the public that after reviewing additional information related to the Ranbaxy atorvastatin recall, FDA has determined that the possibility of adverse health problems related to the recalled atorvastatin is extremely low.

What patients should know . . . "

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World AIDS Day - FDA Voice

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Updated February 15, 2022

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World AIDS Day - CDC.gov

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World AIDS Day | FDA Voice:

"The Food and Drug Administration supports the fight against HIV/AIDS by promoting medical innovation, protecting the blood supply, and reviewing and regulating new and existing medical products, including devices used in prevention, such as condoms and medical gloves. Doctors, nurses, pharmacists, scientists and many others at FDA have worked hard in 2012 to make sure that there are safe and effective medical products and devices available to fight HIV/AIDS."

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