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As of February 2009, the DoD ceased the requirement for IPv6-only testing for certification and entry into the Unified Capabilities Approved Products List (UC APL). According to Kris Strance, DoD CIO IPv6 Lead, "The testing of IPv6 is a part of all product evaluations — it is much broader in scope now." Archived 2010-01-03 at the Wayback ...
A certification listing is a document used to guide installations of certified products. After a field installation is completed, it is compared to the list to make sure that it complies with a regulation (e.g., a building code).
FM 100–5, Operations: 20 August 1982 [19] This publication supersedes FM 100–5, 1 July 1976. Edward C. Meyer: INACTIVE: C1, FM 100–5: FM 100–5, Operations (with included Change No. 1) 29 April 1977 [20] This manual supersedes FM 100–5, 6 September 1968, including all changes. Bernard W. Rogers: INACTIVE: FM 100–5: FM 100–5, Operations
The United States Occupational Safety and Health Administration (OSHA) requires that 38 different types of products, devices, assemblies, or systems used in the workplace be "approved" (i.e., tested and certified) by third-party organizations identified as Nationally Recognized Testing Laboratories (NRTLs). As part of OSHA's NRTL Program, the ...
This is a list of investigational hallucinogens and entactogens, or hallucinogens and entactogens that are currently under formal development for clinical use but are not yet approved. [ 1 ] Chemical/generic names are listed first, with developmental code names, synonyms, and brand names in parentheses.
Type approval or certificate of conformity is granted to a product that meets a minimum set of regulatory, technical and safety requirements. Generally, type approval is required before a product is allowed to be sold in a particular country, so the requirements for a given product will vary around the world.
The FAA published a significant revision to the U.S. manufacturing regulations on October 16, 2009. [17] This new rule eliminates some of the legal distinctions between forms of production approval issued by the FAA, which should have the effect of further demonstrating the FAA's support of the quality systems implemented by PMA manufacturers.
If the Form 356h is missing information, the FDA will reply within 74 days. [3] A BLA asserts that the product is "safe, pure, and potent", the manufacturing facilities are inspectable, and each package of the product bears the license number. Statutory standards for BLA approval are largely the same as those for New Drug Application approval