User:Shawndouglas/sandbox/sublevel2

These addendums to the primary system questionnaire cover system-specific laboratory requirements not common to the laboratory information management system.

1.5 System-specific

1.5a Laboratory information system 1.5a.1 General functions Request for information Requirement code Vendor response a. Does your system include clinical trial management tools? If so, elaborate. b. Does your system provide patient case management and assignment? c. Does your system provide physician, clinic, and contract lab management tools? d. Does your system provide outreach and call list management tools? e. Does your system provide multi-site and multi-lab management tools? f. Does your system provide disease tracking functionality? g. Does your system monitor turnaround time, from test request to clinician review? 1.5a.2 Configuration and customization Request for information Requirement code Vendor response a. Does your system permit users to create templates and worksheets for standardizing analysis pages, patient pages, test ordering pages, and/or the reporting processes? b. Does your system provide flexible and customizable mapping dictionaries for interconversion of different standards and more? c. Does your system support customizable test, panel, and profile libraries? 1.5a.3 Receiving and scheduling Request for information Requirement code Vendor response a. Does your system allow users to create, manage, and track viewable sample container schemata? b. Does your system feature order entry rules for better managing duplicate orders, rejecting inappropriate tests, identifying inappropriate containers, rerouting tests to outside labs, etc.? c. Does your system automatically split and manage orders requiring multiple testing locations? d. Does your system create and manage administrative documents for genetics testing? 1.5a.4 Analysis and data entry Request for information Requirement code Vendor response a. Does your system effectively manage complex molecular protocols? Explain. b. Does your system effectively manage genetic testing protocols? Explain. c. Does your system effectively manage histology and cytology protocols? Explain. 1.5a.5 Post-analysis and validation Request for information Requirement code Vendor response a. Does your system include data mining tools for model learning, evaluation, and usage? a. Does your system report molecular results in both clinical and anatomical pathology environments? 1.5a.6 Instruments Request for information Requirement code Vendor response a. Enter your own unique function here 1.5a.7 External system interfaces Request for information Requirement code Vendor response a. Enter your own unique function here 1.5a.8 Reporting Request for information Requirement code Vendor response a. Does your system include a synoptic reporting module? b. Does your system produce specialized reports for microbiology, hematology, assay trend, and/or cardiac risk? 1.5a.9 Laboratory management Request for information Requirement code Vendor response a. Does your system include revenue management functionality, including medical necessity checks and profitability analysis? 1.5b Electronic laboratory notebook 1.5b.1 Electronic laboratory notebook Request for information Requirement code Vendor response a. Enter your own unique function here 1.5c Chromatography and scientific data management system 1.5c.1 Chromatography and scientific data management system Request for information Requirement code Vendor response a. Enter your own unique function here