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CISPR is the acronym of Comité International Spécial des Perturbations Radio, [1] or the International Special Committee for Radio Protection of IEC. CISPR Standards aim to the protection of radio reception in the range 9 kHz to 400 GHz from interference caused by operation of electrical or electronic appliances and systems in the electromagnetic environment.
Electromagnetic compatibility (EMC) is the ability of electrical equipment and systems to function acceptably in their electromagnetic environment, by limiting the unintentional generation, propagation and reception of electromagnetic energy which may cause unwanted effects such as electromagnetic interference (EMI) or even physical damage to ...
The publication describes requirements, levels and test methods to achieve immunity compliance of an electronic product. The purpose is to create a reproducible ground for product compliance and the standard defines: ranges, levels, test equipment, setups, procedures, calibrations, generator waveforms and general uncertainties.
A TEM or transverse electromagnetic cell is a type of test chamber used to perform electromagnetic compatibility (EMC) or electromagnetic interference (EMI) testing. It allows for the creation of far field electromagnetic fields in a small enclosed setting, or the detection of electromagnetic fields radiated within the chamber.
It necessitates the test of surge immunity in electrical or electronic equipment. IEC 61000-4-5 defines test set-up, procedures, and classification levels. In particular, it standardizes the required surge voltage and current waveforms for laboratory testing, with the "1.2/50-8/20 μs" impulse being the most frequently used surge waveform.
MIL-STD-461 [1] is a United States Military Standard that describes how to test equipment for electromagnetic compatibility.. The United States Department of Defense issued MIL-STD-461 in 1967 to integrate electromagnetic compatibility into the research and development stage for defense communications technology. [2]
An engineering verification test (EVT) is performed on first engineering prototypes, to ensure that the basic unit performs to design goals and specifications. [1] Verification ensures that designs meets requirements and specification while validation ensures that created entity meets the user needs and objectives.
In the pharmaceutical industry, drug dissolution testing is routinely used to provide critical in vitro drug release information for both quality control purposes, i.e., to assess batch-to-batch consistency of solid oral dosage forms such as tablets, and drug development, i.e., to predict in vivo drug release profiles. [1]