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#FDA Issues Proposed Rule to Require Electronic #Drug #Prescribing Information - The FDA said it is proposing that this prescribing information can no longer be distributed in paper form, except as provided by the regulation. The White House Office of Management and Budget has been reviewing the proposed rule since August 2013. http://www.bna.com/fda-issues-proposed-n17179919316/ #fdanews

#FDA Issues Proposed Rule to Require Electronic #Drug #Prescribing Information - The FDA said it is proposing that this prescribing information can no longer be distributed in paper form, except as provided by the regulation. The White House Office of Management and Budget has been reviewing the proposed rule since August 2013. http://www.bna.com/fda-issues-proposed-n17179919316/ #fdanews

#FDA announces Pharmacy Compounding Advisory Committee members - The FDA today announced the membership of the Pharmacy Compounding Advisory Committee. The committee is comprised of 14 members  - 12 voting and two non-voting - who will provide advice on scientific, technical and medical issues concerning drug compounding under sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act. http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm427005.htm

#FDA announces Pharmacy Compounding Advisory Committee members - The FDA today announced the membership of the Pharmacy Compounding Advisory Committee. The committee is comprised of 14 members - 12 voting and two non-voting - who will provide advice on scientific, technical and medical issues concerning drug compounding under sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act. http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm427005.htm

#FDA lodges complaints against five retailers for ‘selling adulterated milk’ - The Food and Drug Administration (FDA), Thane, conducted a special drive against those selling adulterated milk in the market. The FDA had collected 81 samples that were unsafe for consumption, out of which 6 belonged to reputed producers. http://timesofindia.indiatimes.com/city/thane/FDA-lodges-complaints-against-five-retailers-for-selling-adulterated-milk/articleshow/45540322.cms #fdanews

#FDA lodges complaints against five retailers for ‘selling adulterated milk’ - The Food and Drug Administration (FDA), Thane, conducted a special drive against those selling adulterated milk in the market. The FDA had collected 81 samples that were unsafe for consumption, out of which 6 belonged to reputed producers. http://timesofindia.indiatimes.com/city/thane/FDA-lodges-complaints-against-five-retailers-for-selling-adulterated-milk/articleshow/45540322.cms #fdanews

#FDA approves first #biosimilar #drug for distribution in the US - The Food and Drug Administration has approved the first biosimilar drug for distribution in the United States, the agency announced on Friday.  The drug approved was Zarxio, a medication used to prevent infections in cancer patients receiving chemotherapy. www.pbs.org/newshour/rundown/fda-approves-first-biosimilar-drug-distribution-us/

#FDA approves first #biosimilar #drug for distribution in the US - The Food and Drug Administration has approved the first biosimilar drug for distribution in the United States, the agency announced on Friday. The drug approved was Zarxio, a medication used to prevent infections in cancer patients receiving chemotherapy. www.pbs.org/newshour/rundown/fda-approves-first-biosimilar-drug-distribution-us/

#FDA approves Xtoro to treat swimmer’s ear - Acute otitis externa is an infection in the outer ear and ear canal, usually caused by bacteria in the ear canal. Activities in which the ear is underwater can create a moist environment where bacteria may sometimes grow. The infection causes inflammation of the ear canal leading to pain, swelling, redness of the ear and discharge from the ear. http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm427274.htm #fdanews

#FDA approves Xtoro to treat swimmer’s ear - Acute otitis externa is an infection in the outer ear and ear canal, usually caused by bacteria in the ear canal. Activities in which the ear is underwater can create a moist environment where bacteria may sometimes grow. The infection causes inflammation of the ear canal leading to pain, swelling, redness of the ear and discharge from the ear. http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm427274.htm #fdanews

#FDA OKs First Pathogen Reduction System for #Plasma - The US Food and Drug Administration (FDA) has approved the first plasma pathogen reduction system designed to reduce the risk for transfusion-transmitted infections. http://www.medscape.com/viewarticle/836755 #fdanews

#FDA OKs First Pathogen Reduction System for #Plasma - The US Food and Drug Administration (FDA) has approved the first plasma pathogen reduction system designed to reduce the risk for transfusion-transmitted infections. http://www.medscape.com/viewarticle/836755 #fdanews

#FDA faces more scrutiny in #Congress over response to #superbug outbreaks - Joining others in Congress, Sen. Patty Murray has called on the Food and Drug Administration to fully investigate medical scopes tied to recent superbug outbreaks at hospitals across the country. http://www.latimes.com/business/la-fi-fda-superbug-outbreaks-20150311-story.html

#FDA faces more scrutiny in #Congress over response to #superbug outbreaks - Joining others in Congress, Sen. Patty Murray has called on the Food and Drug Administration to fully investigate medical scopes tied to recent superbug outbreaks at hospitals across the country. http://www.latimes.com/business/la-fi-fda-superbug-outbreaks-20150311-story.html

Learn the GMO labeling requirements and FDA policies and regulations regarding GMOs. Attend the webinar by Norma Skolnik.

Learn the GMO labeling requirements and FDA policies and regulations regarding GMOs. Attend the webinar by Norma Skolnik.

#CPR-Assistance System Approved by #FDA - The ResQCPR System includes two devices meant to be used together. One of the devices is called the ResQPump Active Compression Decompression CPR Device. It has a double-grip handle that attaches to the patient's chest with a suction cup, allowing the rescuer to push to deliver compressions and lift for decompressions, which is different than standard CPR. http://www.webmd.com/heart-disease/heart-failure/news/20150309/cpr-assistance-system-fda

#CPR-Assistance System Approved by #FDA - The ResQCPR System includes two devices meant to be used together. One of the devices is called the ResQPump Active Compression Decompression CPR Device. It has a double-grip handle that attaches to the patient's chest with a suction cup, allowing the rescuer to push to deliver compressions and lift for decompressions, which is different than standard CPR. http://www.webmd.com/heart-disease/heart-failure/news/20150309/cpr-assistance-system-fda

7 websites to help you save on health care  -- Prices for procedures and prescriptions are all over the map, and consumers often haven't known what charges would be ahead of time. Now you can go online to find out what to expect. / Jun 6 '13

7 websites to help you save on health care -- Prices for procedures and prescriptions are all over the map, and consumers often haven't known what charges would be ahead of time. Now you can go online to find out what to expect. / Jun 6 '13

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