2.2. List the files and years of CMS data requested at that time and explain how they are used in the analysis. List all the “primary” CMS data (DUA reference 14049) you request and all the derived files (reference to the DUA under which it is currently authorized) that you want to work with. 3. They request research identifiable files (RIF). Why can`t LDS (Limited Data Sets) files be used for this study? Describe why you can only use riF data to complete the study. For more information, see ResDAC. The timeline of ResDAC CMS DUA Application Approval Processes usually lasts at least 3 to 5 months between the deposit and receipt of the data. 2. Have you guaranteed that your data request contains the minimum amount of data needed to achieve your research objectives? List the data needed to complete the workload defined in section 1. The CAD is responsible for tracking and documenting all DUAs and supporting the IRB certificates issued for each project using data hosted on the DAC servers. The DAC Director and the DAC Compliance Coordinator are available to examiners during the DUA submission process.
Data Management Plan The DAC establishes a data management plan and other documents necessary for the submission of the DUA. Please note that in some cases other data/variables may be required. For example, Part D (data on medicinal products subject to medical prescription) requires a specific variable justification. Project staff Send a full list of who (name and contact details) participated in the project to the DAC Compliance Coordinator. Include anyone working with the data, writing papers with the data, and/or supervising someone who will work with the data. 2.1. Please describe how this cohort will complete the minimum required data. Specify the approximate size of the expected cohort (number of Benes) to ensure that you do not exceed a 20% sample of the Carrier file. 5. If you intend to apply for the National Death Index segment of the Master Beneficiary Summary File, please complete the NDI Supplement. Please contact the DAC Director if you intend to work with the National Death Index. Abstract: 1.
Summary of studies. Please complete this section by explaining in detail the scope of work of your project, which usually includes a language specific to the objectives and objectives of the fellowship. Please note that this should be the same volume of work as was submitted in the project review form. Any changes to the scope of work will require the updated approval of the project review form. Dissemination and reporting of results Please indicate to which magazines, presentations, forums, meetings, etc. You want to spread your results. CMS requires certain names such as JAMA, NEJM, Academy Health, etc.