نتایج جستجو برای: food and drug administration fda
تعداد نتایج: 16951772 فیلتر نتایج به سال:
The United States Food and Drug Administration (FDA) ensures that patients in the U.S. have access to safe and effective medical devices. The Division of Neurological and Physical Medicine Devices reviews medical technologies that interface with the nervous system. This article addresses how to navigate the FDA's regulatory landscape to successfully bring medical devices to patients.
aCenter for Biologics Evaluation and Research (CBER), Office of Blood Research and Review (OBRR), Food and Drug Administration (FDA), Rockville, Maryland 20852; b1st Faculty of Medicine and c3rd Faculty of Medicine, Charles University, Prague, Czech Republic; dNational Institutes of Health, Clinical Center, Bethesda, Maryland, 02892; and eNational Institute of Standards and Technology, Gaithers...
Figure 2. Respondents’ ratings to the prompt, “I know and understand the FDA [Food and Drug Administration] indications for TMS [transcranial magnetic stimulation] use in treatment-resistant depression.” Figure 1. Respondents’ ratings to the prompt, “I know how to refer someone for TMS [transcranial magnetic stimulation].” BIDMC, Beth Israel Deaconess Medical Center; MGH, Massachusetts General ...
ACR American College of Radiology, CRCPD Conference of Radiation Control Program Directors, FDA Food and Drug Administration, ICRU International Commission on Radiation Units and Measurements, IEC International Electrotechnical Commission, IRP interventional reference point, Ka,r total air kerma at the interventional reference point, NCRP National Council on Radiation Protection and Measurement...
Oral isotretinoin (13-cis-retinoic acid) was first approved as treatment for severe acne by the US Food and Drug Administration (FDA) in 1982. To date the efficacy of isotretinoin has not been superseded by any other treatment and over two decades later isotretinoin remains the most clinically effective anti-acne therapy, producing long-term remission and/or significant improvement in many pati...
DRUG labeling is of vital importance in guiding the safe and effective use of approved drugs. Drug labels represent the most visible expression of months or years of scientific review by physicians and scientists at the U.S. Food and Drug Administration (FDA), and they are also fundamental to the purpose and mission of the FDA. Creation of the FDA dates to the 1906 passage of the Food and Drugs...
in iran we already use laminate tubes only in cosmetics industry. laminate tube manufacturers via using the most modern technology of the world, faced with the laminate tube market being saturated in cosmetics industry for packaging the cosmetic creams and toothpaste. but considering the great food market and therefore laminate tube features such as beautiful packaging, ease of use for the fina...
Non-small cell lung cancer (NSCLC) poses a serious threat to people’s health. Its morbidity and mortality are among the highest all malignant tumors, there is an urgent need for more effective new treatment methods. In recent years, NSCLC immunotherapy has made great progress, first PD-1 inhibitor nivolumab (Nivolumab, O drug) was approved by US Food Drug Administration (FDA) in March 2015, app...
Aetna considers endoscopic injection of dextranomer/hyaluronic acid copolymer (Deflux), polydimethylsiloxane (Macroplastique), polytetrafluoroethylene (Teflon), or other bulking agents approved by the U.S. Food and Drug Administration (FDA) for vesicoureteral reflux (VUR) medically necessary for the treatment of members with primary or secondary VUR who have any of the following conditions when...
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