![]() ![]() Planning/Evaluation Constraint:The period of time this technology is currently being evaluated, reviewed,Īnd tested in controlled environments. Prohibited: The technology/standard is not (currently) permitted to be used under any circumstances. Additional information on when the entry is projected to become unapproved may beįound on the Decision tab for the specific entry. Has been granted to the project team or organization that wishes to use the technology.ĭivest: VA has decided to divest itself on the use of the technology/standard.Īs a result, all projects currently utilizing the technology/standard must plan to eliminate their use of The Authorizing Official Designated Representative ( AODR) as designated by the Authorizing Official ( AO) or designeeĪnd based upon a recommendation from the POA&M Compliance Enforcement, Unapproved: This technology or standard can be used only if a POA&M review is conducted and signed by In the VA Decision Matrix is considered unapproved for use.Īpproved: The technology/standard has been approved for use.Īpproved w/Constraints: The technology/standard can be used within the specified constraints locatedīelow the decision matrix in the footnote and on the General tab. ![]() Any major.minor version that is not listed To ensure that the target version of the technology will be supported. Responsibility to consult the organizations responsible for the desktop, testing, and/or production environments These decisions areīased upon the best information available as of the most current date. The VA Decision Matrix displays the current and future VA IT position regarding different releases of a TRM entry. TRM Technology, obtained from the vendor (or from the release source). The Vendor Release table provides the known releases for the For additional information or assistance regarding Section 508, please contact the Section 508 Office at DecisionsĬADD Administrator Medication Safety Software PharmGuard MSS Administrator This product is considered Medical Technology as defined by the VA in the Medical Device Isolation Architecture (MDIA). Prior to use of this technology, users should check with their supervisor, Information Security Officer (ISO), Facility Chief Information Officer (CIO), or local Office of Information and Technology (OI&T) representative to ensure that all actions are consistent with current VA policies and procedures prior to implementation. Users must ensure sensitive data is properly protected in compliance with all VA regulations. Users must ensure their use of this technology/standard is consistent with VA policies and standards, including, but not limited to, VA Handbooks 61 VA Directives 6004, 6513, and 6517 and National Institute of Standards and Technology (NIST) standards, including Federal Information Processing Standards (FIPS). This technology uses a Microsoft Structured Query Language (SQL) Server database to store Protocol Libraries, usage logs, and user account information. Note: This evaluation covers only the software associated with the hardware, and not the hardware itself. This technology may also be used to print barcodes and view reports. Additionally, this technology allows administrators to determine the amount of flexibility the point of care user can have in editing protocols. PharmGuard Administrator allows for custom programming of multiple area specific configurations. Protocol libraries allow for simultaneous programmable hard and soft limits for dose, weight, time, and all modes of delivery. This technology allows users to create a series of pump settings and parameters for quick and consistent use by end users. This technology allows protocol administrators to set up protocol libraries for point of care users working with CADD-Solis ambulatory infusion pumps or PharmGuard Point of Care Medication Safety Software. The PharmGuard Administrator Medication Safety Software, previously the CADD-Solis Medication Safety Software, is a medical safety software for Medfusion syringe pumps. More information on the proper use of the TRM can be found on the Provide measured drug therapy to patients in hospital or outpatient settings.Technologies must be operated and maintained in accordance with Federal and Department security and Class 2 Device Recall CADD Solis Ambulatory Infusion PumpĬADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. ![]()
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