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Homologation (Greek homologeo, ὁμολογέω, "to agree") is the granting of approval by an official authority.This may be a court of law, a government department, or an academic or professional body, any of which would normally work from a set of rules or standards to determine whether such approval should be given.
The Presidential Appointment Efficiency and Streamlining Act of 2011 (Pub. L. 112–166 (text)), signed into law on August 10, 2012, eliminates the requirement of Senate approval for 163 positions, allowing the president alone to appoint persons to these positions: [7] Parts of the act went into effect immediately, while other parts took effect ...
Approval rating, a polling term which reflects the approval of a particular person or program; Approval voting, a voting system; Approval proofer, an output device used in Prepress proofing; Approved drug, formal government approval of a medication for sale; Social approval, the positive appraisal and acceptance of a person by a social group
Security clearances can be issued by many United States of America government agencies, including the Department of Defense (DoD), the Department of State (DOS), the Department of Homeland Security (DHS), the Department of Energy (DoE), the Department of Justice (DoJ), the National Security Agency (NSA), and the Central Intelligence Agency (CIA).
This position is defined by the Department of Defense Directive 8500.1 (Information Assurance) - E2.1.13. Designated Approving Authority (DAA). As an example. The National Security Agency (NSA) may recommend to a unified command to operate at a certain classification range; e.g. U.S. Special Operations Command
Approval (in relation to institutional review boards (IRBs)) The affirmative decision of the IRB that the clinical trial has been reviewed and may be conducted at the institution site within the constraints set forth by the IRB, the institution, good clinical practice (GCP), and the applicable regulatory requirements.
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In most countries, a marketing authorisation is valid for a period of 5 years. After this period, one should apply for renewal of the marketing authorisation, usually by providing minimal data proving that quality, efficacy and safety characteristics are maintained and the risk-benefit ratio of the medicinal product is still favourable.