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A cleanroom or clean room is an engineered space that maintains a very low concentration of airborne particulates. It is well isolated, well controlled from contamination , and actively cleansed. Such rooms are commonly needed for scientific research and in industrial production for all nanoscale processes, such as semiconductor manufacturing.
ISO/DIS 14644-1.2(2014): Classification of air cleanliness by particle concentration [4] ISO 14644-2: Specifications for testing and monitoring to prove continued compliance with ISO 14644-1 [3] ISO/DIS 14644-2.2(2014): Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration [5]
The aim of cleanroom suitability tests is to determine the suitability of machines and operating utilities (air conditioning, venting, etc.) for use in cleanrooms. The tests must be carried out using measurement techniques as particle emission behavior cannot be adequately assessed by the naked eye or similar means.
Medical Code of Ethics is a document that establishes the ethical rules of behaviour of all healthcare professionals, such as registered medical practitioners, physicians, dental practitioners, psychiatrists, psychologists, defining the priorities of their professional work, showing the principles in the relations with patients, other physicians and the rest of community.
Cleanliness suitability describes the suitability of operating materials and ventilation and air conditioning components for use in cleanrooms where the air cleanliness and other parameters are controlled by way of technical regulations. Tests are carried out to determine this. [1] [2]
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The International Code of Medical Ethics [1] was adopted by the General Assembly of the World Medical Association at London in 1949, and amended in 1968, 1983, and 2006. It is a code based on the Declaration of Geneva and the main goal is to establish the ethical principles of the physicians worldwide, based on his duties in general, to his patients and to his colleagues.
The Common Rule is a 1991 rule of ethics (revised in 2018) [2] regarding biomedical and behavioral research involving human subjects in the United States.The regulations governing Institutional Review Boards for oversight of human research followed the 1975 revision of the Declaration of Helsinki, and are encapsulated in the 1991 revision to the U.S. Department of Health and Human Services ...