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Wavelet image format used primarily with geo-referenced aerial and satellite imagery No EMF: Enhanced Metafile Format Microsoft.emf, .emz Microsoft Office: EMF+: Enhanced Metafile Format Plus Extensions Microsoft.emf, .emz ERF: EPSON RAW EPSON TIFF .erf Exif: Exchangeable Image File Format .exif EVA Extended Vector Animation Sharp Corporation.eva
Electromagnetic shielding. Electromagnetic shielding cages inside a disassembled mobile phone. In electrical engineering, electromagnetic shielding is the practice of reducing or redirecting the electromagnetic field (EMF) in a space with barriers made of conductive or magnetic materials. It is typically applied to enclosures, for isolating ...
Drolet's 1990 Rhumart system, a PEMF device. Pulsed electromagnetic field therapy ( PEMFT, or PEMF therapy ), also known as low field magnetic stimulation ( LFMS) is the use of electromagnetic fields in an attempt to heal non-union fractures and depression. [1] By 2007 the FDA had cleared several such stimulation devices.
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An EMF meter is a scientific instrument for measuring electromagnetic fields (abbreviated as EMF). Most meters measure the electromagnetic radiation flux density (DC fields) or the change in an electromagnetic field over time (AC fields), essentially the same as a radio antenna, but with quite different detection characteristics.
Counter-electromotive force. Counter-electromotive force ( counter EMF, CEMF, back EMF ), [1] is the electromotive force (EMF) manifesting as a voltage that opposes the change in current which induced it. CEMF is the EMF caused by electromagnetic induction .
ARC – Nintendo U8 Archive (mostly Yaz0 compressed) ARJ – ARJ compressed file. ASS, SSA – ASS (also SSA): a subtitles file created by Aegisub, a video typesetting application (also a Halo game engine file) B – (B file) Similar to .a, but less compressed. BA – BA: Scifer Archive (.ba), Scifer External Archive Type.
Synopsis. The CTD is an internationally agreed format for the preparation of applications regarding new drugs intended to be submitted to regional regulatory authorities in participating countries. It was developed by the European Medicines Agency (EMA, Europe), the Food and Drug Administration and the Ministry of Health, Labour and Welfare ...