PPT-Electronic Controlled Drug Record (CDR)

Author : jane-oiler | Published Date : 2018-11-10

in At the end of this tutorial the nurse will be able to Identify the need for electronic documentation of IV controlled medications Summarize process for the

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Electronic Controlled Drug Record (CDR): Transcript

in At the end of this tutorial the nurse will be able to Identify the need for electronic documentation of IV controlled medications Summarize process for the documentation of and cosignature requirements of IV controlled substances within HED. xisting requirement means the requirement was in the regulations prior to the 2011 modifications Principal reporting year PRY means the latest complete calendar year preceding the submission period ID Description 2006 IUR 2007 2008 2009 2010 2011 P Drug Record (. eCDR. ). in . eCDR. Overview. Controlled Drug Record documentation will be completed in HED instead of on the paper CDR.. Paper CDR will only . be used for . transfers . into or out . Part 1 of a 3 Part Series. Chuck Klein, Ph.D.. GM/Director, Medication Management. Agenda. Defining EPCS. Legal Aspects of EPCS. Pharmacies. Requirements: OrderConnect. Requirements: Prescribers. Two-Factor Authentication. Why Review Your CDR Data. H. igh CDR could result in . Adverse publicity. Loss of Title IV eligibility. Loss of access to private loan funds. Extra work. Administrative capability. Why Review Your CDR Data. Prescriber and Agent Workflow. Part 3 of a 3 Part Series. Chuck Klein, Ph.D.. GM/Director, Medication Management. Agenda. Defining EPCS. Requirements: Prescribers. Workflow for Prescribers . Workflow for Agents. Within the patient’s chart, click on Orders, then CDR to access CDR flowsheet. Customize the flowsheet to display date range or number of days. Select Continuous for frequency of charting. Review chart elements for Start of infusion, q4h charting, and ending of infusion.. Presented by: . David . Guinasso. , Supporting OSD AT&L DPAP. dguinasso@altamconsult.com. January 2017. DRAFT. 1. CDR. What Is It . What is the Policy for Using CDRs. . What Roles Are Available. Richard L. Ogletree, Jr., . PharmD. Co-. ordinator. , Drug Information and Investigational Drugs. University of Mississippi Medical Center. MANP Summer Conference. July . 1. 9. , 2105. Faculty Disclaimer. Presented by: . David Guinasso, Supporting OSD AT&L DPAP. dguinasso@altamconsult.com. Beta. We will Review. What is a Contract Deficiency Report (CDR)? . Why did we change the existing CDR process?. Part 1 of a 3 Part Series. Chuck Klein, Ph.D.. GM/Director, Medication Management. Agenda. Defining EPCS. Legal Aspects of EPCS. Pharmacies. Requirements: OrderConnect. Requirements: Prescribers. Two-Factor Authentication. Russell Dorsey, . CP. h. T. Special Projects/Indigent . C. are . P. rogram . C. oordinator. Baptist Health . M. edical . C. enter – Little Rock. Disclosure. I have no financial interests or other disclosures of conflict of interests for this presentation.. and Their Application. Jeffrey . L. . Privette. (NOAA), . W. Jesse Glance (NOAA),. L. . DeWayne Cecil. (Global . Science and . Technology). &. John J. Bates (NOAA). The Academy View. The National Research Council (NRC, 2004) defines a CDR as a time series of measurements of sufficient length, consistency, and continuity . s. eptember. 2014). P. Valente. , E. . Leonardi. , F. . Pantaleo. Objectives. Re-start CDR for data-taking as it was in 2012-2013. Reverse-engineer the scripts in order to. Fix problems . Control and maintain it as it is. SEMINAR BY. SWAPNA.M. M.PHARMACY. 2. nd. SEMESTER. UNIVERSITY COLLEGE OF PHARMACEUTICAL SCIENCES. KAKATIYA UNIVERSITY,WARANGAL. .

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