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USP 800 (Hazardous Drugs—Handling in Healthcare Settings) is a guideline created by the United States Pharmacopeia Convention (USP), as one of their General Chapters through which the USP "sets quality standards for medicines, dietary supplements and food ingredients".
It has been determined that current personal protective equipment (PPE) does not provide adequate protection against workers handling hazardous drugs - NIOSH states that “... measurable concentrations of some hazardous drugs have been documented in the urine of health care workers who prepared or administered them − even after safety ...
The drug or other substance has a high potential for abuse. The drug or other substance has no currently accepted medical use in treatment in the United States. There is a lack of accepted safety for use of the drug or other substance under medical supervision. The complete list of Schedule I substances is as follows. [1]
The NIOSH definition is the only definition that includes drug vapors. [8] NIOSH considers the containment of vapor extremely important, such that in September 2015, NIOSH issued a Testing Protocol to assess the effectiveness of closed systems. [9] NIOSH developed and tested five CSTDs to assess its "closeness". Two of the five CSTDs tested passed.
This is the list of Schedule II controlled substances in the United States as defined by the Controlled Substances Act. [1] The following findings are required, by section 202 of that Act, for substances to be placed in this schedule: The drug or other substance has a high potential for abuse.
It also maintains List I of chemicals and List II of chemicals, which contain chemicals that are used to manufacture the controlled substances/illicit drugs. The list is designated within the Controlled Substances Act [ 1 ] but can be modified by the U.S. Attorney General as illegal manufacturing practices change.
NIOSH was created by the Occupational Safety and Health Act of 1970 [27] and began operating in May 1971. [25] It was originally part of the Health Services and Mental Health Administration, and was transferred into what was then called the Center for Disease Control (CDC) in 1973. [27] NIOSH's initial headquarters were located in Rockville ...
Tier 2 banding is also incorporated into the NIOSH OEB e-tool but can take hours instead of minutes to complete for a given chemical. However, the resulting band is considered more robust than a Tier 1 band due to the in-depth retrieval of published data. [7] NIOSH recommends users complete at least the Tier 2 process to produce reliable OEBs.