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DIACAP defined a DoD-wide formal and standard set of activities, general tasks and a management structure process for the certification and accreditation (C&A) of a DoD IS which maintained the information assurance (IA) posture throughout the system's life cycle.
This led to the Uniterm indexing system in the early 1950s. In 1963, the group was once again reorganized to become the Defense Documentation Center for Science and Technical Information (DDC), and placed under the direction of the Defense Supply Agency (DSA). The DDC moved to Cameron Station, Alexandria, Virginia. The name changed again in ...
A complete set of the US DoD Rainbow Series computer security documents. The Rainbow Series (sometimes known as the Rainbow Books) is a series of computer security standards and guidelines published by the United States government in the 1980s and 1990s.
Starting with System z9 running z/OS 1.7, IBM offered the multiple-subchannel set facility, which allowed up to four independent sets of 64 Ki subchannels. [ 3 ] The installation was responsible for defining the Input/Output Configuration Data Set s ( IOCDS' s), and the operator could select a specific IOCDS as part of a power on reset (POR).
eMASS is a service-oriented computer application that supports Information Assurance (IA) program management and automates the Risk Management Framework (RMF). [1] The purpose of eMASS is to help the DoD to maintain IA situational awareness, manage risk, and comply with the Federal Information Security Management Act (FISMA 2002) and the Federal Information Security Modernization Act (FISMA ...
The security policy must be explicit, well-defined, and enforced by the computer system. Three basic security policies are specified: [6] Mandatory Security Policy – Enforces access control rules based directly on an individual's clearance, authorization for the information and the confidentiality level of the information being sought.
Design review is also required of medical device developers as part of a system of design controls described in the US Food and Drug Administration's governing regulations in 21CFR820. In 21CFR820.3(h), design review is described as "documented, comprehensive, systematic examination of the design to evaluate the adequacy of the design ...
United States Department of Defense standard 5015.2-STD, the Design Criteria Standard for Electronic Records Management Software Applications, was implemented in June 2002.