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Total Results: 934 records

Showing results for "food".

41. Psn-Pdf (pdf file)
    psnet.ahrq.gov/node/47016/psn-pdf
    June 25, 2018 - Food and Drug Administration Precertification pilot program for digital health software: weighing the … Food and Drug Administration Precertification Pilot Program for Digital Health Software: Weighing the … https://psnet.ahrq.gov/issue/us-food-and-drug-administration-precertification-pilot-program-digital-health … https://psnet.ahrq.gov/issue/us-food-and-drug-administration-precertification-pilot-program-digital-health-software … https://psnet.ahrq.gov/issue/us-food-and-drug-administration-precertification-pilot-program-digital-health-software

42. MedWatch E-list. | PSNet
    psnet.ahrq.gov/issue/medwatch-e-list
    September 29, 2010 - United States Food and Drug Administration; FDA. … Facebook Twitter Linkedin Copy URL March 1, 2010 United States Food … Food and Drug Administration (FDA) resulting from MedWatch reports. … United States Food and Drug Administration; FDA.

43. Psn-Pdf (pdf file)
    psnet.ahrq.gov/node/862996/psn-pdf
    February 21, 2024 - Descriptive analysis on disproportionate medication errors and associated patient characteristics in the Food … Descriptive analysis on disproportionate medication errors and associated patient characteristics in the Food … Using data from the Netherlands’ Food and Drug Administration’s Adverse Event Reporting System (FAERS

44. Human Factors and Medical Devices. | PSNet
    psnet.ahrq.gov/issue/human-factors-and-medical-devices
    July 31, 2012 - Center for Devices and Radiological Health, US Food and Drug Administration. … Copy URL September 27, 2017 Center for Devices and Radiological Health, US Food … Food and Drug Administration (FDA) works with manufacturers to ensure the application of HFE in the design … Center for Devices and Radiological Health, US Food and Drug Administration.

45. Nimodipine Capsules (marketed as Nimotop). | PSNet
    psnet.ahrq.gov/issue/nimodipine-capsules-marketed-nimotop
    September 29, 2010 - Rockville, MD: US Food and Drug Administration; January 1, 2006. … Rockville, MD: US Food and Drug Administration; January 1, 2006. This U.S. … Food and Drug Administration alert reminds health care professionals that nimodipine should only be administered … Rockville, MD: US Food and Drug Administration; January 1, 2006.

46. FDA Guidance Document: Hospital Bed System Dimensional and Assessment Guidance to Reduce Entrapment. | PSNet
    psnet.ahrq.gov/issue/fda-guidance-document-hospital-bed-system-dimensional-and-assessment-guidance-reduce
    July 01, 2009 - Rockville MD: Center for Devices and Radiological Health, Food and Drug Administration: March 10, 2006 … URL October 28, 2010 Rockville MD: Center for Devices and Radiological Health, Food … Food and Drug Administration. … Rockville MD: Center for Devices and Radiological Health, Food and Drug Administration: March 10, 2006

47. Examples of Medical Device Misconnections. | PSNet
    psnet.ahrq.gov/issue/examples-medical-device-misconnections
    March 04, 2015 - Food and Drug Administration. February 23. 2023. … Share Facebook Twitter Linkedin Copy URL March 8, 2023 Food … This series of case studies drawn from reports submitted to the Food and Drug Administration illustrates … Food and Drug Administration. February 23. 2023.

48. Reporting of death in US Food and Drug Administration medical device adverse event reports in categories other than death. | PSNet
    psnet.ahrq.gov/issue/reporting-death-us-food-and-drug-administration-medical-device-adverse-event-reports
    April 07, 2019 - Study Reporting of death in US Food and Drug Administration medical device adverse … Reporting of death in US Food and Drug Administration medical device adverse event reports in categories … Reporting of death in US Food and Drug Administration medical device adverse event reports in categories … February 15, 2023 Use of recalled devices in new device authorizations under the US Food

49. OpenFDA. | PSNet
    psnet.ahrq.gov/issue/openfda
    April 08, 2020 - US Food and Drug Administration; FDA. … Share Facebook Twitter Linkedin Copy URL June 11, 2014 US Food … US Food and Drug Administration; FDA. … Food and Drug Administration Precertification pilot program for digital health software: weighing the

50. Drug manufacturers' delayed disclosure of serious and unexpected adverse events to the US Food and Drug Administration. | PSNet
    psnet.ahrq.gov/issue/drug-manufacturers-delayed-disclosure-serious-and-unexpected-adverse-events-us-food-and-drug
    July 10, 2017 - Drug manufacturers' delayed disclosure of serious and unexpected adverse events to the US Food … Drug Manufacturers' Delayed Disclosure of Serious and Unexpected Adverse Events to the US Food and Drug … Drug Manufacturers' Delayed Disclosure of Serious and Unexpected Adverse Events to the US Food and Drug … A proposed rule by the Food and Drug Administration.

51. Potential Medication Error Risks with Investigational Drug Container Labels. | PSNet
    psnet.ahrq.gov/issue/potential-medication-error-risks-investigational-drug-container-labels
    March 08, 2021 - Citation Text: Reagan-Udall Foundation and US Food and Drug Administration. Public Meeting. … Facebook Twitter Linkedin Copy URL Reagan-Udall Foundation and US Food … Cite Citation Citation Text: Reagan-Udall Foundation and US Food

52. Risk of electromagnetic interference with medical telemetry systems operating in the 460-470 MHz frequency bands. | PSNet
    psnet.ahrq.gov/issue/risk-electromagnetic-interference-medical-telemetry-systems-operating-460-470-mhz-frequency
    October 07, 2021 - Citation Text: Food and Drug Administration; FDA; CDER; Center for Drug Evaluation and Research; MedWatch … Share Facebook Twitter Linkedin Copy URL November 30, 2005 Food … Linkedin Copy URL Cite Citation Citation Text: Food

53. FDA preliminary public health notification: update of information about Ralstonia spp. associated with Vapotherm Respiratory Gas Administration device. | PSNet
    psnet.ahrq.gov/issue/fda-preliminary-public-health-notification-update-information-about-ralstonia-spp-associated
    April 17, 2019 - Citation Text: Food and Drug Administration; FDA. … Share Facebook Twitter Linkedin Copy URL January 11, 2006 Food … Linkedin Copy URL Cite Citation Citation Text: Food

54. Artificial intelligence related safety issues associated with FDA medical device reports. | PSNet
    psnet.ahrq.gov/issue/artificial-intelligence-related-safety-issues-associated-fda-medical-device-reports
    May 29, 2024 - Patient safety reports submitted to the Food and Drug Administration’s (FDA) Manufacturer and User Facility … February 15, 2023 Use of recalled devices in new device authorizations under the US Food … January 25, 2023 Reporting of death in US Food and Drug Administration medical device

55. Psn-Pdf (pdf file)
    psnet.ahrq.gov/node/36243/psn-pdf
    September 06, 2006 - The Food and Drug Administration's National Drug Code Directory. September 6, 2006 Levinson DR. … https://psnet.ahrq.gov/issue/food-and-drug-administrations-national-drug-code-directory This report … https://psnet.ahrq.gov/issue/food-and-drug-administrations-national-drug-code-directory

56. Advocate Redi-Code blood glucose test strips by Diabetic Supply of Suncoast: recall—labeling error. | PSNet
    psnet.ahrq.gov/issue/advocate-redi-code-blood-glucose-test-strips-diabetic-supply-suncoast-recall-labeling-error
    August 05, 2020 - Silver Spring, MD: US Food and Drug Administration; June 11, 2014. … Silver Spring, MD: US Food and Drug Administration; June 11, 2014. … Silver Spring, MD: US Food and Drug Administration; June 11, 2014.

57. FDA public health notification: unretrieved device fragments. | PSNet
    psnet.ahrq.gov/issue/fda-public-health-notification-unretrieved-device-fragments
    June 02, 2021 - Silver Spring MD, Center for Devices and Radiological Health, US Food and Drug Administration; January … March 12, 2019 Silver Spring MD, Center for Devices and Radiological Health, US Food … Silver Spring MD, Center for Devices and Radiological Health, US Food and Drug Administration; January … A proposed rule by the Food and Drug Administration.

58. FDA cautions about dose confusion and medication errors for antibacterial drug Zerbaxa (ceftolozane and tazobactam). | PSNet
    psnet.ahrq.gov/issue/fda-cautions-about-dose-confusion-and-medication-errors-antibacterial-drug-zerbaxa
    April 08, 2020 - Food and Drug Administration; FDA. … Share Facebook Twitter Linkedin Copy URL November 3, 2015 Food … Food and Drug Administration; FDA. … Draft guidance for industry and Food and Drug Administration staff.

59. Psn-Pdf (pdf file)
    psnet.ahrq.gov/node/50814/psn-pdf
    January 22, 2020 - extended-release/long-acting opioid prescribing Risk Evaluation and Mitigation Strategy Program by the US Food … Extended-Release/Long-Acting Opioid Prescribing Risk Evaluation and Mitigation Strategy Program by the US Food … Freedom of Information Act request, researchers investigated the implementation and effectiveness of the Food

60. Safety Considerations for Container Labels and Carton Labeling Design to Minimize Medication Errors: Guidance for Industry. | PSNet
    psnet.ahrq.gov/issue/safety-considerations-container-labels-and-carton-labeling-design-minimize-medication-errors
    January 13, 2021 - Rockville, MD: US Department of Health and Human Services, Food and Drug Administration, Center for Drug … Copy URL May 25, 2022 Rockville, MD: US Department of Health and Human Services, Food … Rockville, MD: US Department of Health and Human Services, Food and Drug Administration, Center for Drug … Draft guidance for industry and Food and Drug Administration staff.