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  2. Amid new disclosures, Iowa’s position on licensing boards ...

    www.aol.com/amid-disclosures-iowa-position...

    Iowa's licensure agency discloses previously withheld facts in a case against a chiropractor. But has it changed its policy? Amid new disclosures, Iowa’s position on licensing boards remains unclear

  3. Medicines and Healthcare products Regulatory Agency

    en.wikipedia.org/wiki/Medicines_and_Healthcare...

    The Medicines Control Agency (MCA) and the Medical Devices Agency (MDA) merged in 2003 to form MHRA. In April 2012, the GPRD was rebranded as the Clinical Practice Research Datalink (CPRD). In April 2013, MHRA merged with the National Institute for Biological Standards and Control (NIBSC) and was rebranded, with the MHRA identity being used for ...

  4. Medtronic - Wikipedia

    en.wikipedia.org/wiki/Medtronic

    Medtronic plc is an American-Irish medical device company. The company's operational and executive headquarters are in Minneapolis, Minnesota, and its legal headquarters are in Ireland due to its acquisition of Irish-based Covidien in 2015.

  5. Iowa Foundation for Medical Care - Wikipedia

    en.wikipedia.org/wiki/Iowa_Foundation_for...

    Iowa Foundation for Medical Care (IFMC) is an American nonprofit organization which provides services in health care quality improvement and medical information management. Taxpayer-funded, [ 1 ] IFMC is based in West Des Moines, Iowa and has offices in Illinois , Maryland and Oklahoma .

  6. Iowa medical board has finalized rules for state's 6-week ...

    www.aol.com/iowa-medical-board-finalized-rules...

    The Iowa Board of Medicine has approved guidelines for Iowa's restrictive abortion law that bans the procedure when cardiac activity is detected. Iowa medical board has finalized rules for state's ...

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  9. Investigational device exemption - Wikipedia

    en.wikipedia.org/wiki/Investigational_Device...

    An investigational device exemption (IDE) allows an investigational device (i.e. a device that is the subject of a clinical study [1]) to be used in order to collect safety and effectiveness data required to support a premarket approval (PMA) application or a premarket notification [510(k)] submission to Food and Drug Administration (FDA). [2]