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Sterile dental instruments from hospital central supply (barcoded label indicating sterilization date, expiry date and contents). The central sterile services department (CSSD), also called sterile processing department (SPD), sterile processing, central supply department (CSD), or central supply, is an integrated place in hospitals and other health care facilities that performs sterilization ...
Decontamination (sometimes abbreviated as decon, dcon, or decontam) is the process of removing contaminants on an object or area, including chemicals, micro-organisms, and/or radioactive substances. This may be achieved by chemical reaction , disinfection , and/or physical removal.
Groundwater remediation is the process that is used to treat polluted groundwater by removing the pollutants or converting them into harmless products. Groundwater is water present below the ground surface that saturates the pore space in the subsurface.
Contamination control is the generic term for all activities aiming to control the existence, growth and proliferation of contamination in certain areas. Contamination control may refer to the atmosphere as well as to surfaces, to particulate matter as well as to microbes and to contamination prevention as well as to decontamination.
Standard Methods For the Examination of Water and Wastewater (21 ed.). American Public Health Association. ISBN 978-0-87553-047-5. Also available on CD-ROM and online by subscription. Masters, Gilbert M.; Ela, Wendell (2008). Introduction to Environmental Engineering and Science. Hoboken, NJ: Prentice Hall. ISBN 9780131481930. EPA.
An effluent decontamination system (EDS) is a device, or suite of devices, designed to decontaminate or sterilise biologically active or biohazardous materials in fluid and liquid waste material.
Dry decontamination is a method of removing contaminants (such as chemicals, biological particles, or other liquids, gasses, or solids) without the need to use water or other liquids. Decontamination is an essential duty of hazmat responders as it protects victims from harmful reactions to the contaminants.
In pharmaceutics, sink condition is a term mostly related to the dissolution testing procedure.. It means using a sheer volume of solvent, usually about 5 to 10 times greater than the volume present in the saturated solution of the targeted chemical (often the API, and sometimes the excipients) contained in the dosage form being tested.