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In quality management, a nonconformity (sometimes referred to as a non conformance or nonconformance or defect) is a deviation from a specification, a standard, or an expectation. Nonconformities or nonconformance can be classified in seriousness multiple ways, though a typical classification scheme may have three to four levels, including ...
A product defect is any characteristic of a product which hinders its usability for the purpose for which it was designed and manufactured. Product defects arise most prominently in legal contexts regarding product safety , where the term is applied to "anything that renders the product not reasonably safe". [ 1 ]
North Carolina's judiciary never attempted to adopt the doctrine, and the state legislature enacted a statute expressly banning strict liability for defective products in 1995. [25] [26]) In a landmark 1986 decision, the U.S. Supreme Court also embraced strict liability for defective products by adopting it as part of federal admiralty law. [27]
Operate a quality surveillance system to sample and test medicines to address quality defects and to monitor the safety and quality of unlicensed products. Investigate internet sales and potential counterfeiting of medicines, and prosecute where necessary. Regulate clinical trials of medicines and medical devices.
In health care the most important resource is your employees. The employees include nurses, CNAs, unit secretaries, housekeepers, laboratory personnel, pharmacists, radiology personnel ...
In legal disputes regarding product liability, a consumer-expectations test is used to determine whether the product is negligently manufactured or whether a warning on the product is defective. Under this test, the product is considered defective if a reasonable consumer would find it defective. The test is typically applied to non-complex ...
Micrometers, voltmeters, automated test equipment (but not equipment used to make the product) Indirect poor-quality costs Customer-incurred cost Loss of productivity due to product or service downtime; Travel costs and time spent to return defective product; Repair costs after warranty period; Backup product or service to cover failure periods
A defect can be defined as a nonconformance of a quality characteristic (e.g. strength, width, response time) to its specification. DPMO is stated in opportunities per million units for convenience: processes that are considered highly capable (e.g., processes of Six Sigma quality) are those that experience fewer than 3.4 defects per million ...