Regulatory Affairs Syndicator

A software failure allowed up to 50mL extra volume of an ingredient to be added to the IV solution that can be life-threatening, particularly in newborns.

HDMA Commends Congressional Enactment Of Food And Drug …Medical News Today (press release), UK - 4 hours agoHDMA commends the US House of Representatives and the Senate for passing the Food and Drug Administration Amendments Act (HR 3580), …

HDMA Commends Congressional Enactment Of Food And Drug …Medical News Today (press release), UK - 12 hours agoHDMA commends the US House of Representatives and the Senate for passing the Food and Drug Administration Amendments Act (HR 3580),…

HDMA Commends Congressional Enactment Of Food And Drug …Medical News Today (press release), UK - 16 hours agoHDMA commends the US House of Representatives and the Senate for passing the Food and Drug Administration Amendments Act (HR 3580),…

HDMA Commends Congressional Enactment Of Food And Drug …Medical News Today (press release), UK - Sep 26, 2007HDMA commends the US House of Representatives and the Senate for passing the Food and Drug Administration Amendments Act (HR 3580),…

Food and Drugs Can Create a Toxic MixU.S. News & World Report, DC - 9 hours agoThe Food and Drug Administration keeps a list of common food and drug interactions. Here are some hazardous mixtures: • Antihistamines: Don't take these …

SpiritIndiaFDA Issues Advisory on Cephalon DrugTheStreet.com - 7 hours agoBy Elizabeth Trotta On Wednesday the Food and Drug Administration issued a public health advisory in light of reports of deaths and other adverse events …FDA issues warnin…

ReutersCaraco gets FDA approval for hyperthyroidism drugDetroit Free Press, United States - 2 hours agoBY ALEJANDRO BODIPO-MEMBA Caraco Pharmaceutical Laboratories Ltd. said it received final US Food and Drug Administration approval for the …

Ahead of the Bell:Fees on imported goodsBusinessWeek - 6 hours ago"We are now importing twice as much food as we were a decade ago, yet the (Food and Drug Administration) examines less than 1 percent of it," Dingell said …

Patients to try Spiration deviceSeattle Post Intelligencer - 3 hours agoA successful outcome will aid the company in obtaining approval from the Food and Drug Administration for approval to market the device commercially, …

FDA Report on Increased Rx Adverse Events Points Americans to …Business Wire (press release), CA - 11 hours ago(BUSINESS WIRE)–Following the publication of a report based upon US Food and Drug Administration data that says serious adverse …

ReutersLabopharm completes enrolment for Phase III clinical study for its …CNNMoney.com - 10 hours agoBased on discussions with US Food and Drug Administration (FDA), Labopharm expects to submit a New Drug Application (NDA) for its once-daily fo…

Food claims are born in Bloomington labsIndianapolis Star, United States - 2 hours ago"We did the pivotal studies (used by) the FDA (Food and Drug Administration) in approving the health claim," said Maki, the company's preside…

A field service technician did not perform all of the hardware Recall: upgrades required in accordance with Baxter?s corrective action procedures related to eight open Colleague recalls. The service technician certified in the service documentation…

Turkish PressDEA Announces Wide-Ranging Steroid BustsThe Associated Press - 1 hour agoThe Internal Revenue Service, US Immigration and Customs Enforcement and the Food and Drug Administration were also involved. In Connecticut, four men were …US…