MMC-Einstein Research IT Forum. November 6, 2017
|
|
|
- Kerrie Holmes
- 6 years ago
- Views:
Transcription
1 MMC-Einstein Research IT Forum November 6, 2017
2 Agenda Updated Training Workflow Reminders Updated Research Billing Policy Research Billing Executive Steering Software updates Studies requiring activation in Velos 2
3 Updated Training Training Principles Include Intro to Research Billing Coordinate the Velos and Epic components PIs and coordinators take the same training New User Training Training required before Velos and Epic access is enabled Refresher Training Webinars Tip sheets
4 Workflow Reminders For studies that include orders/visits in Epic Register patient in Epic Associate patient to study in Velos Schedule patients in Epic (associate to research trial) Place orders in Epic (associate to research trial) Update patient status and dates in Velos Review and assign charges in Epic at least weekly
5 Finance Policy for Research JF17.1 Research Billing Policy recently updated Montefiore Intranet Ø Policies Ø Non-Clinical Policies Ø Administrative Policy and Procedure Manual ØFinance section 85BE2-4AA5-4AC2-B8BF-E55F896B08A0
6 Research Billing Steering and Oversight Senior leadership group to ensure coordinated decision Research leadership MMC revenue cycle leadership Research billing compliance Office of Clinical Trials Montefiore IT
7 Resources to the Research Community for Billing New Research billing unit within MMC Finance Velos team Epic team
8 Coming Software Updates Remove ability to add/update patients within Epic (should be done in Velos) Charge review filter to enable display of only new charges. Research Only study charges automated assignment to research account Optimization Use Epic alerts to identify patients eligible for trial For providers For patients Identify a pilot study for this initiative
9 Studies in Velos Requiring Activation
10 Studies in Velos Requiring Activation
11 Studies in Velos Requiring Activation
12 Studies in Velos Requiring Activation
13 Studies in Velos Requiring Activation
14 Studies in Velos Requiring Activation
15 Studies (2017) Requiring Activation-IRB Approved > 60 days
16 Clinical Research Definitions
17 Next Meeting Monday December 4, 8a to 9a, Price Room 351 Meeting invites for 2018 have been sent out
18 Velos-Epic Processes for Different Types of Clinical Research All IRB Reviewed Studies (Monte/Einstein and BRANY) Non MMC/Einstein PI (e.g. Ferkauf) and non MMC patient No Action Required in Velos MMC/Einstein PI or MMC patients IRB non exempt IRB exempt* IRB Approval Required OCT managed OCT not managed Procedures/consent performed at MMC/Einstein Participants consented Procedures/consent performed only at another institution Consent waived Study Documentation in Velos Study Summary Study Team Verification No Epic Submission No Action Required in Velos Full Study Activation in Velos Study Summary Study Team Verification Study Status Activation Send to Epic if: Interventional (drug/device/treatment) or Epic Orders or Epic Research Visits or Study Participation Flag or Do Not Send to Epic if: No Epic Orders (meds/tests/services) and No Epic Research Visits and No Study Participation Flag (confidential study) Enter study subjects in Velos All Cancer studies Other studies where Velos is needed to track subjects When entering subjects into Velos include all status updates: o Initial Consent Signed o Screening o Enrolled o Active on Tx o Active off Tx o Off study No need to enter study subjects in Velos If not a Cancer study Subjects do not need to be tracked in Velos *IRB exempt studies may include: Educational practices Cognitive testing, Surveys, Interviews Study of existing de-identified data, pathological specimens or diagnostic specimens Contact the IRB Exempt Categories Common Rule 45CRF (b) for more information
19 Velos-Epic Processes for Different Types of Clinical Research Send to Epic if Epic Orders (Meds/Tests/Services) Epic Research Visits Study Participation Flag Enter study subjects in Velos Document Initial Consent Signed status and then document ALL Status updates (Screening->Enrolled->Active on Tx->Off Tx->Off Study) No research associated charges Study flag only NO charge hold & review SOC charges only Epic orders** Epic visits Study flag Charge hold & review at present Automate process with new Epic charge handling rules Mixed SOC and Research charges Epic orders** Epic visits Study flag Charge hold & review & assignment This could be facilitated through creation of billing calendars to preassign SOC vs Research charges Research charges only Epic orders** Epic visits Study flag Charge hold & review at present Automate process with new Epic charge handling rules. **Studies with confidential results Use paper orders/requisitions outside of Epic Follow ancillary department workflow to keep results from filing to Epic
MMC-Einstein Research IT Forum
MMC-Einstein Research IT Forum October 2, 2017 Harry Shamoon, Associate Dean for Clinical & Translational Research Barrett Katz, Executive Director, Office of Clinical Trials Vic Hatcher, Associate Dean
MMC-Einstein Research IT Forum
MMC-Einstein Research IT Forum March 1, 2017 Harry Shamoon, Associate Dean for Clinical & Translational Research Barrett Katz, Executive Director, Office of Clinical Trials Vic Hatcher, Associate Dean
RESEARCH 101: THE KEYS TO GETTING APPROVAL & CONDUCTING RESEARCH AT GRADY. MARCH 22, 2018 Presented By: The Offices of Research & Grant Administration
RESEARCH 101: THE KEYS TO GETTING APPROVAL & CONDUCTING RESEARCH AT GRADY MARCH 22, 2018 Presented By: The Offices of Research & Grant Administration LEARNING OBJECTIVES By the end of the session, you
Human Subject Regulations Decision Charts
Human Subject Regulations Decision Charts September 24, 2004 The Office for Human Research Protections (OHRP) provides the following graphic aids as a guide for institutional review boards (IRBs), investigators,
Ask the Experts Panel
Ask the Experts Panel Compliance in Research Colleen Fritsche, Assistant Director of Office of Animal Care and Use Cassie Myers, Deputy Director of Office of Human Research Ethics Chris Nelson, Director
DANA-FARBER / HARVARD CANCER CENTER STANDARD OPERATING PROCEDURES FOR HUMAN SUBJECT RESEARCH
SOP #: CON-100 Page: 1 of 9 Effective Date: 2/28/17 1. POLICY STATEMENT: The research team is responsible for obtaining and documenting the informed consent of each subject who participates in research.
Maestro Care (Epic) and Clinical Research Updates
Maestro Care (Epic) and Clinical Research Updates Denise Snyder Terry Ainsworth Cory Ennis Duke Office of Clinical Research May 08, 2013 Duke s Complex but Productive Research Environment Duke s 10 schools,
Medicare Coverage Analysis. BWH qualifying study training and discussion
Medicare Coverage Analysis BWH qualifying study training and discussion Research Compliance at BWH ØAt BWH, Research Compliance ensures study teams and institution follow governing authorities interprets
eagreements. Research Agreements Made Easier. eagreements Online Informational
es. Research s Made Easier. es Online Informational Sponsored Programs Administration and Office for Technology Development es. Research s Made Easier. es (ē әˈɡrēmәnts) noun. 1. A web portal that assists
AIS Tip Sheet. Velos Patient Registration
1 Refer to the Velos Epic Integration Velos Requirements for Epic Patient Interface document for more information. You must enter your Username in all lowercase letters, but your password as you would
Changes to the Common Rule
Changes to the Common Rule November 21, 2017 S Joseph Austin, JD, LL.M Corey Zolondek, PhD, CIP Introduction: NOTE: Relative to the Common Rule changes, this presentation does not address requirements
DANA-FARBER / HARVARD CANCER CENTER POLICIES FOR HUMAN SUBJECT RESEARCH TITLE:
POLICY #: EDU-100 Page: 1 of 5 1. POLICY STATEMENT: Individuals who participate in research activities overseen by DF/HCC must satisfy specific training requirements in order to conduct human subject research.
Clinical Trials Where World Class Care Begins
Office of Clinical Trials Clinical Trials Where World Class Care Begins We seek to attract novel, innovative and transformational research and devices to our medical center and its stakeholders, and serve
CLINICAL RESEARCH BILLING 101
CLINICAL RESEARCH BILLING 101 HCCA Research Compliance Conference October 31, 2007 Ann G. Mathias, JD, MHSA Ann E. Mitch-Resignalo, RN, MNEd Prepared September 2007 Updated October 2007 UPMC l University
Study Initiation Meeting
Puerto Rico Clinical and Translational Research Consortium Study Initiation Meeting I. Procedure Title: Study Initiation Meeting II. Overview/Procedure Description: 1. The Clinical Research Resources and
20 STEPS FROM STUDY IDEA INCEPTION TO PUBLISHING RESEARCH/ Evidence-Based Practice
20 STEPS FROM STUDY IDEA INCEPTION TO PUBLISHING RESEARCH/ Evidence-Based Practice Nursing Research/ Evidence-Based Practice Checklist (Version 31 January 2012) Specify the date in the left column when
2/24/2017. Academic Medical Center Compliance: Tips, Traps, and Emerging Best Practices. Structure of Duke Health. Duke University
Academic Medical Center Compliance: Tips, Traps, and Emerging Best Practices Colleen Shannon Chief Compliance and Privacy Officer Structure of Duke Health Duke University Duke University Health System
Objectives. Cancer Registry Abstracting
American American College College of of Surgeons 2013 Content 2014 Content cannot be be reproduced or or repurposed without written permission of of the the American College College of Surgeons. of Surgeons.
Medicare Billing and Reimbursement Essentials for Research
Medicare Billing and Reimbursement Essentials for Research Medical Research Summit Grand Hyatt Hotel, Washington, DC Session 103: Monday, March 19, 2001 Agenda Why is Medicare Billing Compliance Important?
QUALITY ASSURANCE PROGRAM
QUALITY ASSURANCE PROGRAM Elaine Armstrong, MS Quality Assurance Manager PURPOSE Verify accuracy of submitted data Verify compliance with protocol and regulatory requirements Provide educational support
EXEMPT RESEARCH. 1. Overview
EXEMPT RESEARCH 1. Overview Research involving human subjects may be exempt from federal regulations requiring IRB review. The Ohio State University (HRPP) is responsible for determining whether research
Centralized Office of Research
Centralized Office of Research The driving force for creating this model or type of clinical trials office (CTO) at JHS was noncompliance issues in billing. What we discovered was a general lack of education
8/10/2011. Welcome. PRIM&R s Primer on the Advance Notice of Proposed Rulemaking. PRIM&R s Primer on the Advance Notice of Proposed Rulemaking
PRIM&R s Primer on the Advance Notice of Proposed Rulemaking August 10, 2011 1:00-2:00 PM ET 1 Welcome PRIM&R s Primer on the Advance Notice of Proposed Rulemaking Joan Rachlin, JD, MPH Executive Director
REGULATORY AND FUNDING CHANGES FOR HUMAN SUBJECTS RESEARCH
REGULATORY AND FUNDING CHANGES FOR HUMAN SUBJECTS RESEARCH Teri Reiche Director, IRB and IACUC Jessica Viglione OSP Research Administrator So many acronyms. DHHS = Department of Health and Human Services
4.2. Clinical Trial Monitor (or Monitor): The person responsible for monitoring the data on behalf of the sponsor or contract research organization.
SOP #: MON-101 Page: 1 of 6 1. POLICY STATEMENT: The DF/HCC understands that external sponsors are required to monitor the progress of clinical investigations and ensure appropriate research data collection
INTEGRATED DATA ANALYTICS AND CARE WORKFLOW OPTIMIZATION
INTEGRATED DATA ANALYTICS AND CARE WORKFLOW OPTIMIZATION CASE STUDY October 2016 1 AGENDA 1 2 3 INTRODUCTIONS Speaker and System 4 Q+A VALUE OF INTEGRATED DATA Why effective ACOs require EHR, Claims, and
eirb Review Checklist
Start an eirb On-Line Submission Analysis Form Section Review Details Section 1: Study Identification & Personnel Study Identification Look for spelling in both Full and Short title. Make sure dates match
Table of Contents for CCC Toolkit
Section 0.2 Overview Table of Contents for CCC Toolkit This document lists and briefly describes all the tools in the CCC Toolkit in alphabetic order. Time needed: As needed Suggested other tools: How
USING SMART IRB AND SINGLE IRB REVIEW
USING SMART IRB AND SINGLE IRB REVIEW Jeannie Barone Director, HRPO ATTRIBUTES Special thanks to Nichelle Cobb, PhD from University of Wisconsin-Madison for her permission to utilize her slides on SMART
Clinical Research Coordinator - Researcher Startup Tool 1 of 7
Clinical Research Coordinator - Researcher Startup Tool 1 of 7 Mount Sinai Hospital Employees: ITHelpDesk@mountsinai.org 212-241-4357 Sinai Central Account Sinai Central is the system used to manage HR
Setting up a CITI account for users not enrolled at or employed by Georgia Tech. Georgia Institute of Technology December 2016
Setting up a CITI account for users not enrolled at or employed by Georgia Tech Georgia Institute of Technology December 2016 www.citiprogam.org Select REGISTER to establish an account. Affiliate with
Essential Documents It s Not Just a Binder!
Essential Documents It s Not Just a Binder! Kelly Unsworth, MS, CCRC, CIP Director of Research Education & Training Office for Human Subject Protection SCORE June 5, 2014 But What percentage of 2014 (to
Pamela Richtmyer, MGH Research Compliance
Pamela Richtmyer, MGH Research Compliance September 27 - Session 1 Basic overview October 4 - Session 2 Tracking patient care charges Invoices to sponsor Insight Patient Care Corrections October 11 - Session
AN OVERVIEW OF CLINICAL STUDY TASKS AND ACTIVITIES
1 AN OVERVIEW OF CLINICAL STUDY TASKS AND ACTIVITIES Key Clinical Study Tasks and Activities 2 Discussion of Key Tasks and Activities 3 Development of the Clinical Protocol and Study Materials 3 Qualification
Integrating social determinants of health in population health case
Integrating social determinants of health in population health case Amanda Parsons MD, MBA management LEARNING OBJECTIVES Describe the relationship between physical health and the social needs of a high
Dallas Municipal Court Update. Ad Hoc Judicial Nominations Committee April 7 th, 2014
Dallas Municipal Court Update Ad Hoc Judicial Nominations Committee April 7 th, 2014 Purpose To provide an overview of Municipal Court reforms Background Current Status Looking Ahead 2 Background History:
Standard Operating Procedures
Clinical Monitoring and Site Verification Procedure Overview To define the standard procedures for preparation and documentation of site visits for clinical monitoring and spoke verification for any NETT
Single IRB Updates VHRPP NEWS YOU CAN USE JANUARY 22, 2018
Single IRB Updates VHRPP NEWS YOU CAN USE JANUARY 22, 2018 Jenni Beadles, MEd, Single IRB Operations Manager (VHRPP) Bree Burks, RN, MSN, CCRP, Senior Director (VCC) Emily Serdoz, MPA, Manager of Translational
Berkeley Experimental Social Science Laboratory (Xlab) Data Oct 1, 2012
Berkeley Experimental Social Science Laboratory (Xlab) Data Resources @Berkeley Oct 1, 2012 What is the Xlab? The Xlab is an inter-disciplinary research center engaged in (laboratory) experimental work
Mastering Clinical Research April 19, :30 am
Mastering Clinical Research April 19, 2017 7:30 am New Question and Answer Response System Log In Directions Use the following link to access pre and post test questions: http://www.socrative.com/ Click
PACS Module Training Course Catalog and Calendar
PACS Module Training Course Catalog and Calendar Prepared by PACS Training Lead: Kelly Kowalski Reviewed by PACS Training Focus Group 10/3/2016 Agreements Course Name: AGR 1: Submit/Route an Agreement
I was asked to pass this along. Not too many of us use Petty Cash for our subjects, but for those who do, this might be helpful:
January 2009 There has been some confusion noted lately about "safety" vs "efficacy" in clinical trials. In general: "safety tests" are tests that are done to monitor for side effects while "efficacy tests"
From Implementation to Optimization: Moving Beyond Operations
From Implementation to Optimization: Moving Beyond Operations Session 260, March 8, 2018 Scott Aikey, Sr. Director, Core Clinical Applications Children s Hospital of Philadelphia 1 Conflict of Interest
Study Responsibilities. Choose all that apply. f. Draw/collect laboratory specimens
Wichita State University Institutional Review Board (IRB) New Study Application Investigator Information Principal Investigator must be a WSU faculty member. Students and anyone outside of WSU are listed
Presented by NC TraCS Institute UNC Office of Clinical Trials UNC Network of Clinical Research Professionals
ORIENTATION FOR NEW CLINICAL RESEARCH COORDINATORS Presented by NC TraCS Institute UNC Office of Clinical Trials UNC Network of Clinical Research Professionals Overall Agenda for Orientation Module 1:
Recovery Audit Contractors: AHA Perspective. Elizabeth Baskett, Policy, AHA February 23, 2012
Recovery Audit Contractors: AHA Perspective Elizabeth Baskett, Policy, AHA February 23, 2012 Agenda Lay of the Land = Audit Overload RACs (Medicare & Medicaid) MACs ZPICs and OIG and DOJ, oh my! AHA and
Please place your phone line on mute.
We will begin the MaRISS Coordinator Call shortly Please place your phone line on mute. 8/26/2016 2 Overview Missing data Correct dates on Baseline NIHSS Form 24 hour window for consent CRF Forms What
A Multi-Pronged Approach to Improve Provider Satisfaction
A Multi-Pronged Approach to Improve Provider Satisfaction Session 149, March 7, 2018 1-2 p.m. Thomas Selva, MD, CMIO, MU Health Care Bryan Bliven, CIO, MU Health Care 1 Conflict of Interest Thomas Selva,
SHP FOR AGENCIES. 102: Reporting and Performance Improvement. Zeb Clayton Vice President of Client Services. v4.00
SHP FOR AGENCIES 102: Reporting and Performance Improvement Zeb Clayton Vice President of Client Services v4.00 Technical Tips Click the red arrow on the upper left to hide the GoToWebinar control panel
HIC Standard Operating Procedure. For-Cause Audits of Human Research Studies
HIC Standard Operating Procedure For-Cause Audits of Human Research Studies Background As part of the Wayne State University (WSU) Human Investigation Committee s (HIC) Human Research Protection Program,
Clinical Research Coordinator - Researcher Startup Tool 1 of 7
Clinical Research Coordinator - Researcher Startup Tool 1 of 7 Mount Sinai Hospital Employees: ITHelpDesk@mountsinai.org 212-241-4357 Sinai Central Account Sinai Central is the system used to manage HR
Proposal Development Guide
Proposal Development Guide Contents The Proposal Tab... 3 Document Overview Panel... 3 Required Fields for Saving Document Panel... 3 Institutional Fields (Conditionally Required)... 8 Sponsor & Program
UA New Common Rule Implementation
The New Common Rule - What does it all mean? This guide serves to assist University of Arizona researchers to understandthe New Common Rule ( new rule ) and how it will be implemented at the University
USF HRPP Updates October 2017
USF HRPP Updates October 2017 Julie Moore, J.D., M.S. PA, CIP Associate Director, Research Integrity & Compliance Research Integrity and Compliance Revised Common Rule 45 CFR 46 Effective date and compliance
MorCare Infection Prevention prevent hospital-acquired infections proactively
Infection Prevention prevent hospital-acquired infections proactively Enterprise Software and Consulting Solutions for Improved Population Health s Enterprise Software and Consulting Solutions Healthcare
Study Start-Up SS STANDARD OPERATING PROCEDURE FOR PRE-STUDY SITE VISIT (PSSV)
Replaces previous version 203.01: 01 July 2014 Study Start-Up SS 203.01 STANDARD OPERATING PROCEDURE FOR PRE-STUDY SITE VISIT (PSSV) Approval: Nancy Paris, MS, FACHE President and CEO 24 May 2017 (Signature
System to Track and Approve Research STAR Principal Investigator/Proxy User Guide
System to Track and Approve Research STAR Principal Investigator/Proxy User Guide Research Administration 125 Worth Street, 4 th Floor New York, NY 10013 Contents I) BACKGROUND INFORMATION... 3 II) ACCESSING
Madison Health s EMR Journey
A Community Connect Model: Madison Health s EMR Journey with The Ohio State University Wexner Medical Center Michael S. Browning, Madison Health Jennifer Piccione, Madison Health Stacie Gecse, RHIA, The
Singapore Cancer Society
Singapore Cancer Society Research Portal Training Manual Submitting Research Application 1 The Singapore Cancer Society (SCS) Cancer Research Grant aims at delivering holistic patient care and hence it
Washington University Institutional Review Board Policies and Procedures. April 20, 2015
Washington University Institutional Review Board Policies and Procedures April 20, 2015 Table of Contents I. AUTHORITY AND INSTITUTIONAL COMMITMENT... 2 II. APPLICABILITY: ACTIVITIES SUBJECT TO IRB JURISDICTION...
SARASOTA MEMORIAL HOSPITAL CANCER RESEARCH PROGRAM POLICY
PS1006 SARASOTA MEMORIAL HOSPITAL CANCER RESEARCH PROGRAM POLICY TITLE: Satellite Site Management Plan Job Title of Reviewer: POLICY #: EFFECTIVE DATE: REVISED DATE: POLICY TYPE: Elizabeth Carr, R.N.,
U S I N G C T O a t U H N f o r M u l t i - S i t e R e s e a r c h
U S I N G C T O a t U H N f o r M u l t i - S i t e R e s e a r c h How to get ethics approval through CTO for multi-site studies and how to obtain and maintain IA at UHN Today s Agenda 1. What is a Research
Institutional Review Board Standard Operating Procedures. Education and Training on Human Subject Research Date Last Revised: OVERVIEW
Page 1 of 6 Document Number: IRB-P106 Version Number: 1.3 Institutional Official: David Carlisle, MD, PhD Title: Institutional Review Board Standard Operating Procedures Education and Training on Human
UNIVERSITY MEDICAL CENTER NEW ORLEANS RESEARCH REVIEW APPLICATION
UNIVERSITY MEDICAL CENTER NEW ORLEANS RESEARCH REVIEW APPLICATION Submission and Approval Process 1. Submit complete RRC application to Office of Research as early as possible in study process. 2. Quality
Effective Date: November 12, 2015 Policy Number: MHC_RP0306. Corporate Director, HRPP Institutional Official, HRPP
Policy Title: Education and Training In Human Subject Research Effective Date: November 12, 2015 Policy Number: Review Date: November 12, 2015 Section: Revised Date: Administrative Responsibility: Oversight
Subject Screening, Recruitment, and Retention. Tiffany Morrison, MS, CCRP Director, Clinical Trials Rothman Institute
Subject Screening, Recruitment, and Retention Tiffany Morrison, MS, CCRP Director, Clinical Trials Rothman Institute Learning objectives List two sources of potential subjects who can be screening for
Guidelines for Review of Research Involving Human Subjects
Institutional Review Board Assumption College Guidelines for Review of Research Involving Human Subjects Table of Contents: Page General Guidelines........ 1 Scope and Purpose of IRB Review...... 1 Basis
Ethics Committee Composition Roles & Responsibilities. Dr Girish Dayma Dr Sanjay Juvekar KEM Hospital Research Centre Pune
Ethics Committee Composition Roles & Responsibilities Dr Girish Dayma Dr Sanjay Juvekar KEM Hospital Research Centre Pune Outline Introduction Composition Roles & Responsibilities Overview of amendment
12.0 Investigator Responsibilities
12.0 Investigator Responsibilities 12.1 Policy Investigators are ultimately responsible for the conduct of research. Research must be conducted according to the signed Investigator statement, the investigational
Review & Negotiation Process for Sponsor & Investigator Initiated Clinical Trial Agreements
Review & Negotiation Process for Sponsor & Investigator Initiated Clinical Trial Agreements Agenda Background Accessing MediTract Submitting a Workflow Tracking the Process in MediTract Navigating MediTract
S1404: GENERAL DATA MANAGEMENT UPDATES
S1404: GENERAL DATA MANAGEMENT UPDATES SWOG 2018 SPRING GROUP MEETING Krystle Pagarigan, BS Clinical Research Data Coordinator SWOG Statistics and Data Management Center (SDMC) Overview Brief History of
The GCP Perspective on Study Monitoring
The GCP Perspective on Study Monitoring Heidi Judge, CCRP Sr. Clinical Trials Project Manager Clinical Trials Network and Institute Massachusetts General Hospital 1 Overview Monitoring Basics Who, What,
PROJECT SCOPE STATEMENT
PROJECT SCOPE STATEMENT Note: Any work not explicitly included in the Project Scope Statement is implicitly excluded from the project. Project Name: Solutions for Integrated Research Compliance SIRC Prepared
General Administration GA STANDARD OPERATING PROCEDURE FOR Sponsor Responsibility and Delegation of Responsibility
General Administration GA 102.01 STANDARD OPERATING PROCEDURE FOR Sponsor Responsibility and Delegation of Responsibility Approval: Nancy Paris, MS, FACHE President and CEO (17 July 2014) (Signature and
EPIC RESEARCH FAQs FOR MGH REVENUE CYCLE IMPLEMENTATION
EPIC RESEARCH FAQs FOR MGH REVENUE CYCLE IMPLEMENTATION GENERAL 1. What does One Patient/One Record mean for researchers, study staff and patients who participate in research studies? 2. What records feed
Improve Patient Care Utilizing Electronic Whiteboard
Improve Patient Care Utilizing Electronic Whiteboard Presented By: Improve Patient Care Utilizing Electronic Whiteboard Christa Weghorn Performance Improvement Specialist IDEXX Laboratories Steve Safris,
SAINT AGNES MEDICAL CENTER CLINICAL RESEARCH CENTER Fresno, California. STANDARD OPERATING PROCEDURES Institutional Review Board
SAINT AGNES MEDICAL CENTER CLINICAL RESEARCH CENTER Fresno, California STANDARD OPERATING PROCEDURES Institutional Review Board Date Effective: April 26, 2001 Index No. R 1217 Date Last Revised: 0 Date
Boosting Your Bottom Line
Boosting Your Bottom Line Making More Money for Clinics Lisa Clark, MBA NYS Office of Mental Health 7/26/16 Partners in CTAC and MCTAC include: Agenda Introduction Review of Revenue Maximization Basics
Aligning Health IT with Delivery System Reform: Technology Gaps in Coordinating Patient Care
Aligning Health IT with Delivery System Reform: Technology Gaps in Coordinating Patient Care Peggi M. Czinger MPH Director, Network Care Management COE The Care Management Company of Montefiore The Bronx:
Study Management PP STANDARD OPERATING PROCEDURE FOR Safeguarding Protected Health Information
PP-501.00 SOP For Safeguarding Protected Health Information Effective date of version: 01 April 2012 Study Management PP 501.00 STANDARD OPERATING PROCEDURE FOR Safeguarding Protected Health Information
Innovations & Brainstorming. Peer to Peer
Innovations & Brainstorming Peer to Peer Innovations and Brainstorming Enrollment Best Practices, Amanda Lee, Children's Medical Center UTSW PK/PD Blood Samples, Kyle Pimenta, UC Davis Children's Hospital
Research Audits PGR. Effective: 12/04/2013 Reviewed: 12/04/2015. Name of Associated Policy: Palmetto Health Administrative Research Review
Effective: 12/04/2013 Reviewed: 12/04/2015 Name of Associated Policy: Palmetto Health Administrative Research Review Definitions Responsible Positions Equipment Needed Procedure Steps, Guidelines, Rules,
New Problem List Dictionary (IMO) Workflow Recommendations
Catherine Hill, RN May 15, 2014 The Problem List Overview What is SNOMED-CT? Mapping ICD SNOMED One-to-one (Bulk mapping) One-to-many (Manual mapping) Mapping Required Basic Navigation Data Display Grid
Industry: Healthcare. Location: Washington, USA. Application: medical records
Hospital Links Meditech and DocuWare CaseStudy Local Washington hospital implements DocuWare to link information entered into their Health Information System, Meditech, with other crucial healthcare documents
Welcome to Maccabi Healthcare Services. Varda Shalev MD MPA ISRAEL
Welcome to Maccabi Healthcare Services Varda Shalev MD MPA ISRAEL Maccabi s Vision Israel's leading and most advanced healthcare organization aims to achieve Total Health for its members, providing integrative
Parkland Health & Hospital System Department of Pathology Research Support
Parkland Health & Hospital System Department of Pathology Research Support The Road to Successful Request for Pathology Research Services Kim Coston, MT(AMT) Pathology Research & Client Services Coordinator
Executive Summary: Davies Ambulatory Award Community Health Organization (CHO)
Davies Ambulatory Award Community Health Organization (CHO) Name of Applicant Organization: Community Health Centers, Inc. Organization s Address: 110 S. Woodland St. Winter Garden, Florida 34787 Submitter
PROSpect The PRone and OScillation Pediatric Clinical Trial
PROSpect The PRone and OScillation Pediatric Clinical Trial http://www.prospect-network.org/ Ancillary Studies Guidelines An ancillary study is defined as an investigation involving PROSpect subjects using
Meaningful Use Key Dates
Meaningful Use Key Dates July 1: Last day for eligible hospitals to begin their 90-day reporting to demonstrate Meaningful Use for FY 2014. Sept. 30: Last day of the federal fiscal year. Proposed Rule-2014
Using Data to Yield High Impact Business Intelligence Wednesday, July 25, 2012
Using Data to Yield High Impact Business Intelligence Wednesday, July 25, 2012 Brent J. Estes President and CEO, Rush Health About Rush Rush University Medical Center 673 Beds 36,000 admissions 391,700
A Bigger Bang Patient Portal Strategy: How we activated 100K patients in our First Year
A Bigger Bang Patient Portal Strategy: How we activated 100K patients in our First Year Saturday March 25 th, 2017 Lindsay Altimare, MPA Director, LVPG Operations Lehigh Valley Health Network Michael Sheinberg,
The Future of Access: A Patient-Centric Vision NAHAM Presentation
The Future of Access: A Patient-Centric Vision 2014 NAHAM Presentation Presenters Karen Shaffer-Platt Georgina Trunzo Vice President, Revenue Cycle/Patient Concierge Services at UPMC 25 years experience
Research-Related Subject Injury: Findings and Lessons Learned from Implementation of a New Policy
Research-Related Subject Injury: Findings and Lessons Learned from Implementation of a New Policy HCCA Research Compliance Conference - Baltimore, MD Breakout Session 302 June 6, 2016 2:30-4:00 PM Keren
Final Rule Material: Overview
Final Rule Material: Overview - 46.116-46.124 Gary L. Chadwick, PharmD, MPH, CIP University of Rochester (Emeritus) and HRP Consulting Group Biomedical Research Alliance of New York LLC CITI Program is
DOC # EPIC ELECTRONIC MEDICAL RECORD ONLINE MANUAL DOWNLOAD
25 April, 2018 DOC # EPIC ELECTRONIC MEDICAL RECORD ONLINE MANUAL DOWNLOAD Document Filetype: PDF 531.94 KB 0 DOC # EPIC ELECTRONIC MEDICAL RECORD ONLINE MANUAL DOWNLOAD An Epic Journey Toward a Fully
NursingCAS Learning & Networking Workshop
Welcome Dallas, TX Texas Woman s University 11:00 AM 2:30 PM Speakers: Caroline Allen, NursingCAS Director, the American Association of Colleges of Nursing Ann Donnelly, Account Management Director for
Catherine Porto, MPA, RHIA, CHP Executive Director HIM. Madelyn Horn Noble 3M HIM Data Analyst
1 Catherine Porto, MPA, RHIA, CHP Executive Director HIM Madelyn Horn Noble 3M HIM Data Analyst University of New Mexico Hospitals» The state s only academic medical center» The primary teaching hospital
Kentucky Sepsis Summit. August 2016
1 Kentucky Sepsis Summit August 2016 St. Elizabeth Healthcare About Us: - 7 facilities & over 1200 licensed beds - Serving the NKY/Cincinnati Region in: - Orthopedic Care - Heart and Vascular Institute
Improving Quality Outcomes in a Risk-Based World: A Davies Story Session #100, March 7, 2018
Improving Quality Outcomes in a Risk-Based World: A Davies Story Session #100, March 7, 2018 David Cloyed, MS, RN-BC, Applications Manager, Nebraska Medicine Tammy Winterboer, PharmD, BCPS, Director, Clinical
Spring User Conference May Sandestin, FL Detailed Agenda
Day One: Monday May 16, 2016 3 6 p.m. Conference Registration 5 6 p.m. Customer Welcome and Orientation for First-time Conference Attendees 6 8 p.m. Welcome Reception Day Two: Tuesday May 17, 2016 7 a.m.