Implementation and Operation of CDISC ODM-based EDC by UMIN

Size: px
Start display at page:

Download "Implementation and Operation of CDISC ODM-based EDC by UMIN"

Transcription

1 Implementation and Operation of CDISC ODM-based EDC by UMIN Takahiro Kiuchi, M.D., Ph.D. UMIN Center, The University of Tokyo Hospital, Tokyo, Japan 1

2 Content 1. CDISC standards and academic research 2. What is UMIN and UMIN INDICE? 3. Implementation and operation of CDISC ODM-based EDC by UMIN 4. Practical development and operation of a real clinical trial by CDISC ODM-based EDC with Fukushima Prefectural University Hospital 2

3 1. CDISC standards and academic research 3

4 What is CDISC? CDISC: Clinical Data Interchange Standards Consortium (Non-profit organization for standardization) Mission: The CDISC mission is to develop and support global, platform-independent data standards that enable information system interoperability to improve medical research and related areas of healthcare. (cited from CDISC website) Members: Pharma, CRO, IT Vendors 4

5 CDISC Standards 1. SDTM Study Data Tabulation Model (SAS.xpt) 2. SEND Standard Exchange for Non-clinical Data (SAS.xpt) 3. ADaM Analysis Dataset Model (SAS.xpt) NDA 4. CRT-DDS Case Report Tabulation and Data Definition Specification (PDF or XML) 5. ODM Operational Data Model (XML) 6. LAB Clinical Laboratory Model (ASCII, SAS.xpt, or XML) 7. PR Protocol Representation (UML) Data transfer 8.CDASH Clinical Data Acquisition Standards Harmonization (Standardized variables for CRF) Study design 5

6 CDISC Standards for regulatory clinical trials Hospital CDASH (Variable names) PR (Protocol) Lab Trial use in U.S.A. and Europe ODM (XML) Lab (XML) (XML) Clinical laboratory company Pharma SDTM SEND ADaM Practical use in U.S.A. SDTM (Clinical) SEND (Non-clinical) ADaM (Statistical analysis) SAS xpt CRT-DDS (Metadata) PDF or XML Regulatory agency SDTM SEND ADaM 6

7 CDISC Standards for academic research Hospital Academic data center Academic publishers CDASH (Variable names) PR (Protocol) Lab ODM (XML) Lab (XML) (XML) Clinical laboratory company SDTM ADaM Paper CDISC Standards can be used for academic clinical trials and epidemiological studies as they are. 7

8 CDISC Standards and ICH EMA PMDA FDA ICH CDISC Standards (Individual clinical data) A Pharma B Pharma C Pharma 8

9 CDISC Standards for FDA, Pharma, Hospital FDA Pharma CDISC Standards Recommendation ->Obligation Data conversion CDISC SDTM Proprietary clinical data management system CDISC SDTM CDISC Standards Recommendation ->Obligation CDISC Standards compatible clinical data management system CDISC Standards Recommendation ->Obligation CDISC SDTM CDISC Standards compatible clinical data management system CDISC ODM Hospital Vendor proprietary data interface for clinical research Vendor proprietary data interface for clinical research CDISC ODM data interface for clinical research 9

10 2. What is UMIN and UMIN INDICE? 10

11 UMIN (University hospital Medical Information Network) Important information infrastructure for academic activities in biomedicine Versatile academic information services, including research, education, and clinical practice National University Hospital Council The Univ. of Tokyo Hospital Control 320 thousands Registered users 50 million page views per month 11

12 UMIN Services -Overview Research AC Academic societies and meetings database ELBIS Electronic Library for Biomedical Sciences FIND Fund Information Database INDICE Internet Data and Information Center ROCOLS Recruiting System for Our Colleagues and Students CTR ICMJ-accredited clinical trial registry Clinical practice Intoxication database (Yamaguchi Univ.) HIV manual (Hokkaido Univ.) Drug information database Drug information text database for pharmacists Medical supplies and materials database Education EPOC Online evaluating system of post-graduate clinical training for physicians Debut Online evaluating system of post-graduate clinical training for dentists Web-QME Web-based Quality Management system for Educational effectiveness VHP Visible Human Project image data University hospitals Official documents database University hospitals guide Master database for patient fee calculation Standardized disease nomenclature database Mailing lists Member-only homepages Multipurpose Information and database services Collection of biomedical web sites Medical terms glossary Research institutes and hospitals database Homepage etc. hosting services Open homepage hosting service Member-only homepage hosting service Archival homepage hosting service Wiki Blog VOD hosting service Communication support services service, including encrypted Mailing list service BBS service Online voting system 12

13 UMIN INDICE (Internet Data and Information Center for Clinical Research) Largest internet clinical research data center in Japan SaaS = Software as a Service UMIN INDICE Data collection Original software package for clinical and epidemiological research User management Internet Information Homepage hosting service Security Communication Mailing list managementsystem Hardware 13

14 Usage statistics of UMIN INDICE research projects One million of registered cases Accummulated Under operation April-00 April-02 April-04 April-06 April-08 April-10 0 Apr-00 Apr-02 Apr-04 Apr-06 Apr-08 Apr-10 14

15 Web-based data collection by UMIN Hospital UMIN Center Web browser Manual entry of digitalized laboratory and drug prescription data (laborious and vulnerable to miss transcription) Electronic Health Record Internet Web-based UMIN INDICE Laboratory data Drug prescription 15

16 3. Implementation and operation of CDISC ODM-based EDC by UMIN 16

17 Web-based data collection by UMIN Hospital UMIN Center Web browser Manual entry of digitalized laboratory and drug prescription data (laborious and vulnerable to miss transcription) Electronic Health Record Internet Web-based UMIN INDICE Laboratory data Drug prescription 17

18 Procedure for developing CDISC ODM-based EDC in UMIN 1. Analysis of a protocol and CRFs 2. Development of web-based EDC server system 3. Development of routine which processes CDISC ODMbased data and accommodate them to web-based EDC server system 4. Development of routine which extract trial data from web-based EDC server system and create CDISC ODMbased data. 5. Development of templates of CDISC ODM which are sent from hospitals to UMIN. 18

19 Hospital Web browser CDISC ODM and Web-based data collection by UMIN (2009/11/6) UMIN Center Manual entry of digitalized laboratory and drug prescription data (laborious and vulnerable to miss transcription) Electronic Health Record Internet Web-based CDISC ODMbased UMIN INDICE Laboratory data Drug prescription Full or semi-automated fulfillment of digitalized laboratory and drug prescription data Entry of other data from electronic health record 19

20 UMIN needs partner hospitals for CDISC ODM-based EDC UMIN could receive CDISC ODM data in early But were there any hospitals which develop CDISC ODM-based research data submission system linked to EHR, using their own funds? => There were two university hospitals! 20

21 Implemention strategy for development of CDISC ODM-based research data submission system linked to EHR Data automatically or semi-automatically collected from EHR are limited to demographic, laboratory, and drug prescription data, which usually covers more than half of trial data. RFD (Retrieve Form for Data), which is based on XForm technology, is not used because the technology is immature and the implementation cost is expensive. 21

22 Implementation procedure for development of CDISC ODM-based research data submission system linked to EHR 1. Development of CRF entry system CRF entry system TP 4.5mg/dl Manual entry 2. Development of a routine for automated or semi-automated fulfillment of demographic, laboratory, and drug prescription data TP 4.5mg/dl Cr 1.1mg/dl Automated entry 3. Development of a routine for checking CRF data TP 4.5mg/dl Cr 1.1mg/dl TC mg/dl Deficit check 4. Development of a routine for creating CDISC ODM from CRF data 5. Submission of CDISC ODM-based data CDISC CDISC ODM ODM-based data submission Conversion to CDISC ODM TP 4.5mg/dl Cr 1.1mg/dl TC110mg/dl 22

23 Packaging Future perspective of the development of CDISC ODM-based research data submission system linked to EHR 1. Proprietary implementation of each hospital for each trial 2. Vendor packaging 1)Vendor-specific module installed by a vendor for each trial 2)Vendor-specific module installed by a hospital for each trial 3)Vendor-specific module automated installed online for each trial 4)CDISC standardized module automated installed online for each trial Development in most EHR vendors Interoperability of CDISC ODM 23

24 4. Practical development and operation of a real clinical trial by CDISC ODM-based EDC with Fukushima Prefectural University Hospital 24

25 Overview of the clinical trial Title Effect of topping up of Toremifene to preoperative chemotherapy of breast cancer Principal investigators Seiichi Takenouchi and Tohru Ohtake The number of cases planned 20 cases The number of participant institutions 7 hospitals, including Fukushima Prefectural Univ. Hospital The study start date Nov. 9 th,

26 EHR and CRF data entry form EHR CRF data entry form Automated fulfillment 26 10

27 Using Yahgee for the implementation(1) What is Yahgee 1)Software tool Data entry forms can be developed and corrected by users themselves (hospitals). 2)Interface for most EHRs sold in Japan Data can be entered and extracted from most EHRs sold in Japan through Yahgee. Yahgee Yahgee interface Yahgee Yahgee interface Yahgee Yahgee interface A company s EHR B company s EHR C company s EHR 27

28 Using Yahgee for the implementation(2) UMIN INDICE Web interface CDISC ODM interface CDISC ODM interface CDISC ODM interface CDISC ODM interface CDISC ODM interface Yahgee Yaghee intereface Yahgee Yaghee interface A company s EHR P hospital B company s EHR Q hospital A company s EHR Fukushima Prefectural Univ. hospital B company s EHR R hospital 28

29 Why the real clinical trial, based on CDISC ODM, realized in Japan first. Realized as an academic (non-profit) clinical trial It is difficult to realize a real EDC in regulatory data collection, using new and immature technology like CDISC Standards. CDISC Standards are misunderstood as those for only new drug application. In fact, their scope are much wider now. Pharma companies concern obligatory CDISC-based new drug application over CDISC-based EDC. Web-based academic EDC system - UMIN INDICE Practical approach for the development of CDISC ODM-based research data submission system linked to EHR 1) Data collected from EHR are limited to demographic, laboratory, and drug prescription data. 2) RFD (Retrieve Form for Data) is not used because the technology is immature and the implementation cost is expensive. 29

30 Thank you for your attention. The presenter s doctor thesis Research on the Use of World Wide Web for a Data Management System for Use in Multi-institutional Clinical Trials Published papers related to the doctor thesis 1) Kiuchi T, Ohashi Y, Konishi M, Bandai Y, Kosuge T, Kakizoe T: A World Wide Web-based user interface for a data management system for use in multiinstitutional clinical trials - Development and experimental operation of an automated patient registration and random allocation system. Controlled Clinical Trials 17: , ) Kiuchi T, Kaihara S: C-HTTP - The development of a secure, closed HTTPbased network on the Internet. Proceedings of the 1996 Symposium on Network and Distributed System Security, IEEE Computer Society Press, 64-75, ) Kiuchi T, Kaihara S: Automated generation of a World Wide Web-based data entry and check program for medical applications. Computer Methods and Programs in Biomedicine 52: ,

The use of electronic Health Records in Clinical Research - The value of CDISC Standards

The use of electronic Health Records in Clinical Research - The value of CDISC Standards The use of electronic Health Records in Clinical Research - The value of CDISC Standards FH-Prof. Dr. Jozef Aerts University of Applied Sciences FH Joanneum Graz, Austria Who is Jozef Aerts? CDISC volunteer

More information

October, Integration and Implementation of CDISC Standards

October, Integration and Implementation of CDISC Standards Integration and Implementation of CDISC Standards October, 2008 Barbara Lentz, Associate Director, Electronic Data Management Standards, Processes & Training Pat Majcher, Statistical Reporting Services

More information

CDASH Clinical Data Acquisition Standards Harmonization

CDASH Clinical Data Acquisition Standards Harmonization CDISC Italian User Group Meeting 16 November 2007 CDASH Clinical Data Acquisition Standards Harmonization 1 Outline Background Organization Goals Timelinesand Process Review of progress Results Future

More information

Chapter 1. Pharmaceutical Industry Overview

Chapter 1. Pharmaceutical Industry Overview Chapter 1 Pharmaceutical Industry Overview 1.1 Introduction 2 1.2 Regulations 2 1.2.1 Health Insurance Portability and Accountability Act 2 1.2.2 The Code of Federal Regulations 3 1.2.3 Guidance for Industry

More information

End-to-End Management of Clinical Trials Data

End-to-End Management of Clinical Trials Data End-to-End Management of Clinical Trials Data A Revolutionary Step Toward Supporting Clinical Trials Analysis Over the Next Decades of Clinical Research WHITE PAPER SAS White Paper Table of Contents Introduction....

More information

CDISC Data Standards Validation

CDISC Data Standards Validation CDISC Data Standards Validation How can it be done? Peter Van Reusel Business Unit Director Business & Decision Life Sciences Tel +32 2 774 11 00 Fax +32 2 774 11 99 Mobile +32 476 54 59 17 peter.vanreusel@businessdecision.com

More information

CDISC UK Network face to face Reading

CDISC UK Network face to face Reading CDISC UK Network face to face Reading Paul Houston, CDISC Head of European Operations CDISC Update and European Activity 2 CDISC Values and Principals Core value Foster CDISC community is altruistic

More information

Aepodia is a team of experts with more than 15 years

Aepodia is a team of experts with more than 15 years Aepodia is a team of experts with more than 15 years experience in early clinical development and translational science with small startup and large global pharmaceutical companies. Aepodia s team has

More information

Data Integrity in Clinical Trials the Sponsor Perspective

Data Integrity in Clinical Trials the Sponsor Perspective Data Integrity in Clinical Trials the Sponsor Perspective Maximilian Stroebe, GSK Vaccines Three differences to Commercial Manufacturing Long process chains Source Data, Clinical Sites and Outsourcing

More information

CDASH 2.0. Berlin Éanna Kiely CDISC Engineer

CDASH 2.0. Berlin Éanna Kiely CDISC Engineer CDASH 2.0 Berlin Éanna Kiely CDISC Engineer 2016-09-13 Agenda CDASH 1.1 & CDASHIG 2.0 CDASH Concepts TAUG Examples Current Regulatory Perspective on CDASH Questions 2 CDASH: CDISC End to End Clinical Data

More information

Laboratory Information Management System Index

Laboratory Information Management System Index Laboratory Information Management System Index About LIMS Patient Tracking Overview Key Module & Key Features LIMS Architecture Benefits LIMS Standards Interface Integration Sample Tracking LIMS. Net Screen-shots

More information

CDISC Customer Requirements Analyses

CDISC Customer Requirements Analyses Data Model Customer Requirements Analyses Copyright 2003 About The Clinical Data Interchange Standards Consortium () is an open, multidisciplinary, non-profit organization committed to the development

More information

Statistical Review and Data Standards: It s Gettin Better All The Time

Statistical Review and Data Standards: It s Gettin Better All The Time Statistical Review and Data Standards: It s Gettin Better All The Time Steve Wilson, Dr.P.H., CAPT USPHS Office of Biostatistics FDA/OMPT/CDER 2017 PharmaSUG Baltimore, MD May 17, 2017 Disclaimer This

More information

Devices, Big Data, and Real World Evidence O R A C L E W H I T E P A P E R O C T O B E R

Devices, Big Data, and Real World Evidence O R A C L E W H I T E P A P E R O C T O B E R Devices, Big Data, and Real World Evidence O R A C L E W H I T E P A P E R O C T O B E R 2 0 1 7 Disclaimer The following is intended to outline our general product direction. It is intended for information

More information

LOINC in Regulated Clinical Research a Lab LOINC Steeringg Committee Meeting 08 June 2017

LOINC in Regulated Clinical Research a Lab LOINC Steeringg Committee Meeting 08 June 2017 LOINC in Regulated Clinical Research a Lab LOINC Steeringg Committee Meeting 08 June 2017 Lauren Becnel, Ph.D. VP, Biomedical Informatics & Alliances, CDISC Asst Prof, Duncan Comprehensive Cancer Center,

More information

Dictation & Transcription Solutions

Dictation & Transcription Solutions Dictation, Transcription, Speech Recognition, Computer-Assisted Coding & CDI Solutions Dictation & Transcription Solutions Highly customizable and completely integrated, crucial components essential for

More information

GeriMedProfiles. Consultant Pharmacist Software

GeriMedProfiles. Consultant Pharmacist Software GeriMedProfiles Consultant Pharmacist Software Features GerimedProfiles TM is a comprehensive medical database for clinical pharmacists Utilizes Microsoft Access as the core database allowing the end-user

More information

Electronic Health Records and Clinical Data Interchange Standards

Electronic Health Records and Clinical Data Interchange Standards Electronic Health Records and Clinical Data Interchange Standards Stephen E. Wilson, Dr.P.H., CAPT USPHS Director Division of Biostatistics III Center for Drug Evaluation and Research US Food and Drug

More information

The Situation of Investigator Initiated Trials in Europe. Dr.N.Gökbuget

The Situation of Investigator Initiated Trials in Europe. Dr.N.Gökbuget The Situation of Investigator Initiated Trials in Europe Dr.N.Gökbuget Investigator Initiated Trials in Europe Difficulties and Possibilities 1. Situation for academic clinical trials after the EU directive

More information

Working with Health IT Systems is available under a Creative Commons Attribution-NonCommercial- ShareAlike 3.0 Unported license.

Working with Health IT Systems is available under a Creative Commons Attribution-NonCommercial- ShareAlike 3.0 Unported license. Working with Health IT Systems is available under a Creative Commons Attribution-NonCommercial- ShareAlike 3.0 Unported license. Johns Hopkins University. Welcome to Health Management Information Systems,

More information

Quality Assurance in Clinical Trials

Quality Assurance in Clinical Trials Quality Assurance in Clinical Trials Doctor Catherine CORNU, Lyon clinical Investigation Centre EUDIPHARM December 5th, 2011 1 Introduction: quality in clinical research in human subjects Regulatory requirements:

More information

Electronic Healthcare Record and Clinical Research in Cardiovascular Radiology. HL7 CDA and CDISC ODM Interoperability

Electronic Healthcare Record and Clinical Research in Cardiovascular Radiology. HL7 CDA and CDISC ODM Interoperability Electronic Healthcare Record and Clinical Research in Cardiovascular Radiology. HL7 CDA and CDISC ODM Interoperability A. El Fadly a, C. Daniel ab, C. Bousquet ab, T. Dart b, P-Y. Lastic c, P. Degoulet

More information

DICTATION & TRANSCRIPTION

DICTATION & TRANSCRIPTION DICTATION & TRANSCRIPTION www.dolbey.com INFO@DOLBEY.com 800 878 7828 Fusion Voice Digital Dictation The quality of a patient s chart relies upon the clinician s ability to effectively communicate findings,

More information

To begin from the beginning

To begin from the beginning POST-AUTHORISATION STUDIES IN EUROPE: BRIDGING THE GAP BETWEEN REGULATORY AND HEALTH TECHNOLOGY ASSESSMENT (HTA) STAKEHOLDER NEEDS BY BETTER DESIGN OF STUDIES Massoud Toussi Epidemiology, Europe Real World

More information

EAUTIFUL BDATA AGGREGATION EXTRAVAGANZA. Implementing a Clinical Data Repository and Analytics Platform in 90 Days

EAUTIFUL BDATA AGGREGATION EXTRAVAGANZA. Implementing a Clinical Data Repository and Analytics Platform in 90 Days DATA IS SIMPLY EAUTIFUL BDATA AGGREGATION EXTRAVAGANZA This artful imagery is an abstract representation of data coming from a myriad of sources to create a single, impactful image. Created by data artist,

More information

PharmaSUG Paper PO12

PharmaSUG Paper PO12 PharmaSUG 2016 - Paper PO12 CDISC Standards End-to-End: Transitional Hurdles Alyssa Wittle, Chiltern International, King of Prussia, PA Christine McNichol, Chiltern International, King of Prussia, PA Antonio

More information

Good Clinical Practice (GCP) & Clinical Trial Registries

Good Clinical Practice (GCP) & Clinical Trial Registries Good Clinical Practice (GCP) & Clinical Trial Registries The Fifth Annual Pharmaceutical Regulatory and Compliance Congress and Best Practice Forum November 14-17, 2004 Kate Maloney, RN, MS, CPHQ Manager,

More information

E2B(R3): THE INSIDE SCOOP FOR PRODUCT SAFETY TEAMS IN LIFE SCIENCES

E2B(R3): THE INSIDE SCOOP FOR PRODUCT SAFETY TEAMS IN LIFE SCIENCES E2B(R3): THE INSIDE SCOOP FOR PRODUCT SAFETY TEAMS IN LIFE SCIENCES PREPARING FOR E2B(R3) T he electronic transmission of adverse event information to stakeholders, using the International Conference on

More information

Welcome to the American College of Toxicology s Webinar Series. We will begin at 11AM EDT

Welcome to the American College of Toxicology s Webinar Series. We will begin at 11AM EDT Welcome to the American College of Toxicology s Webinar Series We will begin at 11AM EDT Preparing for Nonclinical edata Regulatory Submissions to the US FDA SEND and Beyond September 5, 2013, 11:00 AM

More information

Business Process Management (BPM) system SimBASE 4 Introduction June 2015

Business Process Management (BPM) system SimBASE 4 Introduction June 2015 4 [ r ] e v o l u t i o n Business Process Management (BPM) system SimBASE 4 Introduction June 2015 Contents Part 1: What is SimBASE 4 Part 2: Architecture and technologies Part 3: User interfaces Part

More information

EHR Site Visit Questionnaire

EHR Site Visit Questionnaire HIM 3014 Health Information Technology Practicum EHR Assessment - Site Visit Questionnaire Student Name: Instructions: Schedule an EHR site visit and complete the following questionnaire by the date found

More information

Work Package IV Version 1 3/20/2013

Work Package IV Version 1 3/20/2013 Glossary Sl.No Terminology Description 1 Client The direct consumer and beneficiary of a health service (for example patient, women, man, child) 2 Frontline Health Worker Typically community-level health

More information

MEANINGFUL USE CRITERIA PHYSICIANS

MEANINGFUL USE CRITERIA PHYSICIANS MEANINGFUL USE CRITERIA PHYSICIANS The first list is of the 25 Stage 1 Meaningful Use criteria for eligible providers (EP) and comes from the proposed rule: "Medicare and Medicaid Programs; Electronic

More information

Sunshine on Europe: impact of recent EFPIA and EU guidelines on publication planners. Susan Scott, PhD, CMPP Director, Scott Pharma Solutions Ltd

Sunshine on Europe: impact of recent EFPIA and EU guidelines on publication planners. Susan Scott, PhD, CMPP Director, Scott Pharma Solutions Ltd Sunshine on Europe: impact of recent EFPIA and EU guidelines on publication planners Susan Scott, PhD, CMPP Director, Scott Pharma Solutions Ltd Disclaimer As an independent consultant, the views expressed

More information

ReadySet is the Best Kept Secret. GoPaperless with the Industry s ONLY Paperless Solution.

ReadySet is the Best Kept Secret. GoPaperless with the Industry s ONLY Paperless Solution. ReadySet is the Best Kept Secret. GoPaperless with the Industry s ONLY Paperless Solution. 21st Century Solutions for Occupational Health. Workflow Focused ReadySet is a subscription-based solution using

More information

REQUEST for the EuroRec Seal - Seal Level 2 Supplier Form

REQUEST for the EuroRec Seal - Seal Level 2 Supplier Form REQUEST for the Seal - Seal Level 2 Supplier Form This form needs to be completed and signed by the supplier requesting a Seal for an application. The application can be a complete EHR system with a complete

More information

April 13, Background

April 13, Background Pfizer Inc 235 East 42nd Street New York, NY 10017-5755 Tel 212 733 4210 Fax 646 383 9249 Email: marc.wilenzick@pfizer.com April 13, 2009 http://www.regulations.gov Christine Ireland Committee management

More information

POLICY AND PROCEDURE MANUAL

POLICY AND PROCEDURE MANUAL POLICY AND PROCEDURE MANUAL PBRC: POLICY NO. 378.00 ORIGIN DATE: 5/25/2016 IMPACTS: CLINICAL RESEARCH LAST REVISED: 1/1/2017 SUBJECT: SOURCE: PURPOSE PENNINGTON BIOMEDICAL CLINICALTRIALS.GOV POLICY INSTITUTIONAL

More information

Q-STRESS CARDIAC STRESS TESTING SYSTEM

Q-STRESS CARDIAC STRESS TESTING SYSTEM Q-STRESS CARDIAC STRESS TESTING SYSTEM This product is available through: JRT Associates 800-221-0111 A Legacy of Clinical Excellence Mortara brings proven expertise to the forefront of diagnostic cardiac

More information

Advanced Claim Management for GE Customers. Cathrina Caldwell, CPC, CPC-H Director, Sales Product Consulting

Advanced Claim Management for GE Customers. Cathrina Caldwell, CPC, CPC-H Director, Sales Product Consulting Advanced Claim Management for GE Customers Cathrina Caldwell, CPC, CPC-H Director, Sales Product Consulting Agenda Optum Overview Traditional hospital claim workflow A better way Claims Manager Facility

More information

Using local RWD to drive global therapeutic advancements.

Using local RWD to drive global therapeutic advancements. Using local RWD to drive global therapeutic advancements. Helsinki, 30 th Nov 2016 Mike Spencer, Head of Real World Evidence, EMEA, Janssen The following represent my own views and not necessarily those

More information

Integration of EHRs with CDISC, CDASH and ODM A European Initiative

Integration of EHRs with CDISC, CDASH and ODM A European Initiative Budapest, Hungary 22nd 23rd April 2009 Session 2 11:00-12:30 European perspective of EHR integration Chair: Udo Siegmann (Parexel) Integration of EHRs with CDISC, CDASH and ODM A European Jozef Aerts XML4Pharma

More information

Stay Ahead of the Curve in Radiation Reduction Standards

Stay Ahead of the Curve in Radiation Reduction Standards Radiation mandates are coming... MR Suite CT Suite I/Dx Suite Nuclear Suite Stay Ahead of the Curve in Radiation Reduction Standards New NEXO Dose: Radiation aggregation technology that measures multiple

More information

SOA in the pan-canadian EHR

SOA in the pan-canadian EHR SOA in the pan-canadian EHR Dennis Giokas Chief Technology Officer Solutions Products and Group Canada Health Infoway Inc. 1 Outline Infoway EHR Solution EHRS Blueprint Overview Oriented Architecture Business

More information

Lexmark esf Applications. Product Demonstration Guide

Lexmark esf Applications. Product Demonstration Guide Lexmark esf Applications Product Demonstration Guide Description Lexmark s Embedded Solution Framework (esf): Is an application platform that resides on the Lexmark devices Allows java-based applications

More information

Sharing current and archived patient data in the EMC Federation Enterprise Hybrid Cloud

Sharing current and archived patient data in the EMC Federation Enterprise Hybrid Cloud White Paper Patient Records in the Cloud Sharing current and archived patient data in the EMC Federation Enterprise Hybrid Cloud ECD Healthcare Abstract This white paper describes a solution that shows

More information

PharmaSUG 2017 Paper DS14

PharmaSUG 2017 Paper DS14 PharmaSUG 2017 Paper DS14 Considerations in Submitting Standardized Electronic Data Under the Animal Rule: The Use of SDTMIG and SENDIG Domains, and the Need for New Domains and Concepts Fred Wood, Accenture

More information

Create interoperability in a MEDITECH environment

Create interoperability in a MEDITECH environment Create interoperability in a MEDITECH environment Create real connections with your medical community Corepoint Health solutions are transforming the way hospitals and clinics meet their interoperability

More information

FDA Experience with the Sentinel Common Data Model: Addressing Data Sufficiency

FDA Experience with the Sentinel Common Data Model: Addressing Data Sufficiency FDA Experience with the Sentinel Common Data Model: Addressing Data Sufficiency Michael D. Nguyen, MD Office of Surveillance and Epidemiology Center for Drug Evaluation and Research US Food and Drug Administration

More information

esource Advancement Roundtable

esource Advancement Roundtable Clinical Research on FHIR Amy Nordo MMCi, BSN, RN, CPHQ, LNC Duke University Supported in part by Duke s CTSA grant (UL1TR001117) esource Advancement Roundtable August 2017 Duke University 3 Integrated

More information

Optimizing the Vascular Lab: What Are the Benefits and Drawbacks of Currently Available Database Packages? David L. Dawson, MD, RVT, RPVI

Optimizing the Vascular Lab: What Are the Benefits and Drawbacks of Currently Available Database Packages? David L. Dawson, MD, RVT, RPVI Optimizing the Vascular Lab: What Are the Benefits and Drawbacks of Currently Available Database Packages? David L. Dawson, MD, RVT, RPVI DISCLOSURES David Dawson, MD No relevant financial relationship

More information

PCORI Methodology Standards: Academic Curriculum Patient-Centered Outcomes Research Institute. All Rights Reserved.

PCORI Methodology Standards: Academic Curriculum Patient-Centered Outcomes Research Institute. All Rights Reserved. PCORI Methodology Standards: Academic Curriculum 2016 Patient-Centered Outcomes Research Institute. All Rights Reserved. Module 5: Architecture for Data Networks Category 7: Data Networks as Research-Facilitating

More information

Roadmap for Managing Multiple CRO Vendors

Roadmap for Managing Multiple CRO Vendors PharmaSUG 2017 - Paper PO27 Roadmap for Managing Multiple CRO Vendors Veena Nataraj, Shire, Lexington, MA Karin LaPann, Shire, Lexington, MA ABSTRACT When working with CROs, the relationship established

More information

Management of Clinically Significant Device Attributes not Contained in the GUDID: Augmented Unique Device Identifier Data AUDI

Management of Clinically Significant Device Attributes not Contained in the GUDID: Augmented Unique Device Identifier Data AUDI Management of Clinically Significant Device Attributes not Contained in the GUDID: Augmented Unique Device Identifier Data AUDI Report of the MDEpiNet AUDI Workgroup MISSION: Provide the framework for

More information

Data Quality and Integrity: From Clinical Monitoring to Marketing Approval

Data Quality and Integrity: From Clinical Monitoring to Marketing Approval Data Quality and Integrity: From Clinical Monitoring to Marketing Approval Nancy Detich, Ph.D., C.C.R.P. Senior Scientist, Clinical Strategy 18 November 2010 1 Objectives Identify the importance of accuracy,

More information

Constructing Rural Health Information Systems for Critical Access Hospitals:

Constructing Rural Health Information Systems for Critical Access Hospitals: Constructing Rural Health Information Systems for Critical Access Hospitals: Imposing Interoperability on Disparate Legacy Information Systems, Developing Electronic Health Records, and Connecting Rural

More information

Design of Information Systems 1st Lecture

Design of Information Systems 1st Lecture Design of Information Systems 1st Lecture Evaluation method http://online.ase.ro http://sinf.ase.ro Final grade: 50% seminar grade (minimum 5) 50% course grade 1 st written test (in the 6 th week): 2p

More information

Specific pathologist responses for Standard for Exchange of Nonclinical Data (SEND)

Specific pathologist responses for Standard for Exchange of Nonclinical Data (SEND) J Toxicol Pathol 2017; 30: 201 207 Review Specific pathologist responses for Standard for Exchange of Nonclinical Data (SEND) Atsushi Watanabe 1, 2*, Osamu Kusuoka 1, Norihiro Sato 1, Osamu Nakazono 1,

More information

Connecting Cardiac Device Data and the EHR

Connecting Cardiac Device Data and the EHR Learn More Interested in learning more about how Paceart s device management functionality can work in an EHR environment and help you in your move toward the paperless transfer of data? Connecting Cardiac

More information

TOTAL CANCER CARE: CREATING PARTNERSHIPS TO ADDRESS PATIENT NEEDS

TOTAL CANCER CARE: CREATING PARTNERSHIPS TO ADDRESS PATIENT NEEDS TOTAL CANCER CARE: CREATING PARTNERSHIPS TO ADDRESS PATIENT NEEDS William S. Dalton, PhD, MD CEO, M2Gen & Director, Personalized Medicine Institute, Moffitt Cancer Center JULY 15, 2013 MOFFITT CANCER CENTER

More information

Regist ry Vendor Assessm ent

Regist ry Vendor Assessm ent Regist ry Vendor Assessm ent April, 2014 Completed by the (NQRN ) The PCPI Foundation and the disclaim any liability for use or non-use of this document. The PCPI does not provide medical, legal, financial,

More information

Validating electronic source data in clinical trials

Validating electronic source data in clinical trials Controlled Clinical Trials 25 (2004) 437 446 www.elsevier.com/locate/conclintrial Validating electronic source data in clinical trials Ronald G. Marks* Department of Biostatistics, College of Medicine,

More information

Clinical Trial Outsourcing: A Case Study For Small Biotechnology Companies Operating Globally

Clinical Trial Outsourcing: A Case Study For Small Biotechnology Companies Operating Globally Clinical Trial Outsourcing: A Case Study For Small Biotechnology Companies Operating Globally Cerus Corporation Concord, CA Laurence Corash, MD Chief Medical Officer Meisa Propst, Associate Director Clinical

More information

LIAISON ALLOY HEALTH PLATFORM

LIAISON ALLOY HEALTH PLATFORM PRODUCT OVERVIEW LIAISON ALLOY HEALTH PLATFORM WELCOME TO YOUR DATA-INSPIRED FUTURE THE LIAISON ALLOY HEALTH PLATFORM Healthcare and life sciences organizations are struggling to deal with unprecedented

More information

Recommendations for Strengthening the Investigator Site Community

Recommendations for Strengthening the Investigator Site Community Recommendations for Strengthening the Investigator Site Community October 2017 CTTI MISSION: To develop and drive adoption of practices that will increase the quality and efficiency of clinical trials

More information

The EFGCP Report on The Procedure for the Ethical Review of Protocols for Clinical Research Projects in Europe (Update: April 2011) Bulgaria

The EFGCP Report on The Procedure for the Ethical Review of Protocols for Clinical Research Projects in Europe (Update: April 2011) Bulgaria The Procedure for the Ethical Review of Protocols for Clinical Research Projects in Europe (Update: April 2011) Bulgaria Question 1: What laws or regulations apply to an application for conducting a clinical

More information

Clinical Research at MSU

Clinical Research at MSU Financial Administration Development Program: Clinical Research at MSU Kristen Burt, Office of Regulatory Affairs (ORA) Sharon Schooley, Clinical & Translational Sciences Institute (CTSI) February 24,

More information

1 The Clinical Research Coordinator (CRC)... 1

1 The Clinical Research Coordinator (CRC)... 1 TABLE OF CONTENTS Dedication... iii Introduction... xi 1 The Clinical Research Coordinator (CRC)... 1 Role and Responsibilities of the CRC...1 Personality and Skills... 3 Where Do CRCs Work?... 3 CRC Responsibilities...

More information

International Transfers of Personal Data at sanofi-aventis R & D

International Transfers of Personal Data at sanofi-aventis R & D International Transfers of Personal Data at sanofi-aventis R & D Pierre-Yves Lastic, PhD Senior Director, Standards Management & Data Privacy Sanofi-aventis R&D CONFERENCE ON INTERNATIONAL TRANSFERS OF

More information

Study Files and Filing

Study Files and Filing Study Files and Filing The current version of all Hillingdon Hospital R&D Guidance Documents and Standard Operating Procedures are available from the R&D Intranet and Internet sites: www.ths.nhs.uk/departments/research/research.htm

More information

POLOPOLY V9 TECHNICAL OVERVIEW. System Architecture Templates and Presentation Modules

POLOPOLY V9 TECHNICAL OVERVIEW. System Architecture Templates and Presentation Modules POLOPOLY V9 TECHNICAL OVERVIEW System Architecture Templates and Presentation Modules 2008 Atex Group Ltd Polopoly, Polopoly Content Manager, Polopoly Relationship Manager, Polopoly User Module, Polopoly

More information

Power Digital Imaging

Power Digital Imaging OfficePACS Power Digital Imaging Power Unleashed Organize According to Workflow PowerGroup allows physicians to organize studies by key fields and customize the PatientFinder to the way they work. Find

More information

Information Services & New Jersey Sales Tax

Information Services & New Jersey Sales Tax Information Services & New Jersey Sales Tax About New Jersey Taxes Publication ANJ-29 Introduction The retail sale of information services received by customers in New Jersey is subject to New Jersey Sales

More information

Guidance for Industry - Computerized Systems Used in Clinical Trials

Guidance for Industry - Computerized Systems Used in Clinical Trials Page 1 of 14 Regulatory Information Computerized Systems Used in Clinical Trials Guidance for Industry - Computerized Systems Used in Clinical Trials

More information

The Role of Standards in U.S. FDA Regulation of Cellular Therapy Products

The Role of Standards in U.S. FDA Regulation of Cellular Therapy Products The Role of Standards in U.S. FDA Regulation of Cellular Therapy Products Judith Arcidiacono M.S. International Regulatory Expert Standards Development Activities Liaison U.S. Food and Drug Administration

More information

TECSYS Benefits. Improve margin performance. Optimize preference cards. Free up operating room time. Reduce inventory value and wastage

TECSYS Benefits. Improve margin performance. Optimize preference cards. Free up operating room time. Reduce inventory value and wastage useit in the OR TECSYS Benefits Improve margin performance Optimize preference cards Reduce inventory value and wastage Free up operating room time Capacity to manage evidence-based PPI standardization

More information

FDA > CDRH > CFR Title 21 Database Search

FDA > CDRH > CFR Title 21 Database Search Seite 1 von 7 FDA Home Page CDRH Home Page Search A-Z Index 510 (k) Registration Listing Adverse Events PMA Classification CLIA CFR Title 21 Advisory Committees Assembler Recalls Guidance Standards New

More information

Establishment of Clinical Trial Infrastructure

Establishment of Clinical Trial Infrastructure Taiwan s Strategy in the Establishment of Clinical Trial Infrastructure Chei-Hsiang Chen, Ph. D. Director, Biotechnology and Pharmaceutical Industries Program Office, Ministry of Economic Affairs, Taiwan

More information

Intralinks Studyspace : Electronic Investigator-Controlled Site File (eisf)

Intralinks Studyspace : Electronic Investigator-Controlled Site File (eisf) Intralinks Studyspace : Electronic Investigator-Controlled Site File (eisf) Introduction Intralinks Studyspace: Electronic Investigator-Controlled Site File (eisf) Intralinks Studyspace eisf solution is

More information

Compliance mechanisms available in Russia to ensure adherence to ethical guidelines

Compliance mechanisms available in Russia to ensure adherence to ethical guidelines Compliance mechanisms available in Russia to ensure adherence to ethical guidelines Prof. Olga Kubar, Saint Petersburg Pasteur Institute, Russia 1 Project full title: Project acronym: Type of funding scheme:

More information

LINEE GUIDA IN MEDICINA. Corso di Informatica Medica

LINEE GUIDA IN MEDICINA. Corso di Informatica Medica Università degli Studi di Trieste Corso di Laurea Magistrale in INGEGNERIA CLINICA LINEE GUIDA IN MEDICINA Corso di Informatica Medica Docente Sara Renata Francesca MARCEGLIA Dipartimento di Ingegneria

More information

} SolovatSoft healthcare connectivity abilities and experience Overview

} SolovatSoft healthcare connectivity abilities and experience Overview SolovatSoft HL7 experience and projects } What is Hl7? Health Level Seven is one of several American National Standards Institute (ANSI) - accredited Standards Developing Organizations (SDOs) operating

More information

PharmaSUG PO14

PharmaSUG PO14 PharmaSUG 2014 - PO14 Route to SDTM Implementation in In-Vitro Diagnostic Industry: Simple or Twisted Carey Smoak, Roche Molecular Systems, Inc., Pleasanton, CA Sofia Shamas, MaxisIT Inc., NJ Chowdagam

More information

Creating, Managing and Delivering Regulated Content in Pharma. Jim Nichols VP, US Operations & Life Sciences DitaExchange Inc.

Creating, Managing and Delivering Regulated Content in Pharma. Jim Nichols VP, US Operations & Life Sciences DitaExchange Inc. Creating, Managing and Delivering Regulated Content in Pharma Jim Nichols VP, US Operations & Life Sciences DitaExchange Inc. DitaExchange simplifies the way organizations Create Manage Deliver Re-use

More information

Professor Kimme Hyrich, MD, PhD, FRCPC, UK

Professor Kimme Hyrich, MD, PhD, FRCPC, UK GaBI Scientific Meetings 26 January 2017, Pullman London St Pancras, London, UK ROUNDTABLE ON REGISTRIES Practical Considerations for Registries making them work Professor Kimme Hyrich, MD, PhD, FRCPC,

More information

Use of Electronic Health Records to Facilitate Colorectal Cancer Screening Recommendations for Improvement

Use of Electronic Health Records to Facilitate Colorectal Cancer Screening Recommendations for Improvement The following recommendations were proposed, following the September 25 th, 2015 National Colorectal Cancer Roundtable meeting, Improving Electronic Health Records (EHRs) to Support the Delivery of (CRC),

More information

Protection of Research Participants: The IRB Process and the Winds of Change

Protection of Research Participants: The IRB Process and the Winds of Change Protection of Research Participants: The IRB Process and the Winds of Change Ethics in Patient-Oriented Research October 12, 2011 Sharon Friend Director, OHRPP Overview Charge and Function of the IRB Quick

More information

SMe-Plug Software for SME Logistics Operations with e-freight Capability

SMe-Plug Software for SME Logistics Operations with e-freight Capability SMe-Plug Software for SME Logistics Operations with e-freight Capability Martin CW Lai LSCM R&D Centre 18 Sep 2014 1 The SMe-Plug Software Software system to connect to common logistics service platforms

More information

Pharmacovigilance and the Generic Industry. Mark Vieder RPh MBA Director, Safety & Medical Writing Biorasi

Pharmacovigilance and the Generic Industry. Mark Vieder RPh MBA Director, Safety & Medical Writing Biorasi and the Generic Industry Mark Vieder RPh MBA Director, Safety & Medical Writing Biorasi Disclaimer: This presentation has been prepared by Biorasi, LLC solely for the purpose of sharing information and

More information

Analyzing which software needs to be utilized to ensure a timely and more automated process

Analyzing which software needs to be utilized to ensure a timely and more automated process Clinical Data Integration & Management March 20 th Program Day One 08:15 Registration and refreshments 08:50 Chair s opening remarks Analyzing which software needs to be utilized to ensure a timely and

More information

GCP Basics - refresher

GCP Basics - refresher p. 01 GCP Basics - refresher Agenda: p. 02 Brief History of GCP GCP Regulations Principles of ICH E6 Sponsor Responsibilities Computer Systems Common Compliance Issues Brief History of GCP 3 Brief History

More information

Building a Hosted Statistical Computing Environment: Is it Possible?

Building a Hosted Statistical Computing Environment: Is it Possible? PharmaSUG2011 - Paper DM01 Building a Hosted Statistical Computing Environment: Is it Possible? John Leveille, d-wise Technologies, Raleigh, NC, USA ABSTRACT Small pharmaceutical companies face a large

More information

Functional Requirements for Enterprise Clinical Data Management: Solving Technical Problems, Satisfying User Needs

Functional Requirements for Enterprise Clinical Data Management: Solving Technical Problems, Satisfying User Needs Functional Requirements for Enterprise Clinical Data Management: Solving Technical Problems, Satisfying User Needs All around the world, regulatory requirements and market forces are driving a growing

More information

IHE IT Infrastructure (ITI) Technical Framework Supplement. Cross-Enterprise Document Workflow (XDW) Draft for Public Comment

IHE IT Infrastructure (ITI) Technical Framework Supplement. Cross-Enterprise Document Workflow (XDW) Draft for Public Comment Integrating the Healthcare Enterprise 5 IHE IT Infrastructure (ITI) Technical Framework Supplement 10 Cross-Enterprise Document Workflow (XDW) 15 Draft for Public Comment 20 Date: June 3, 2011 Author:

More information

EFPIA layperson summary Principles that apply to Clinical Trial Transparency. Antonio Ferrari (Chiesi) & Solange Rohou (AZ)

EFPIA layperson summary Principles that apply to Clinical Trial Transparency. Antonio Ferrari (Chiesi) & Solange Rohou (AZ) EFPIA layperson summary Principles that apply to Clinical Trial Transparency. Antonio Ferrari (Chiesi) & Solange Rohou (AZ) Disclaimer I am an employee of Chiesi Farmaceutici s.p.a (Head of Clinical Safety

More information

What s New in HL7. W. Ed Hammond, PhD Director, Duke Center for Health Informatics FACMI, FAIMBE, FHL7, FIMIA Secretary, HL7; Chair-Emeritus, HL7

What s New in HL7. W. Ed Hammond, PhD Director, Duke Center for Health Informatics FACMI, FAIMBE, FHL7, FIMIA Secretary, HL7; Chair-Emeritus, HL7 What s New in HL7 W. Ed Hammond, PhD Director, Duke Center for Health Informatics FACMI, FAIMBE, FHL7, FIMIA Secretary, HL7; Chair-Emeritus, HL7 In the beginning HL7 s initial venture into creating standards

More information

HEALTHCARE. Taking workflow where you want it to go.

HEALTHCARE. Taking workflow where you want it to go. HEALTHCARE Taking workflow where you want it to go. The evolution of Healthcare IT has reached medical imaging. Single Integrated Database Konica Minolta s Exa Platform offers a unique and unparalleled

More information

Good Clinical Practice

Good Clinical Practice Dublin Academic Medical Centre Good Clinical Practice Patrick Murray, MD, FASN, FRCPI Professor, University College Dublin, Mater Misericordiae University Hospital, Dublin, Ireland patrick.murray@ucd.ie

More information

Clinical Data Acquisition Standards Harmonization (CDASH)

Clinical Data Acquisition Standards Harmonization (CDASH) Clinical Data Acquisition Standards Harmonization () Prepared by: CDISC Team Section Table of Contents Page 1.0 Orientation... 1 1.1 Purpose... 1 1.2 Organization of this Document... 1 1.2.1 General Notes...2

More information

Incentives and Regulatory Considerations in Orphan Drug/Medical Device Development - Situation in Japan -

Incentives and Regulatory Considerations in Orphan Drug/Medical Device Development - Situation in Japan - Incentives and Regulatory Considerations in Orphan Drug/Medical Device Development - Situation in Japan - MHLW/PMDA, Japan Speaker: Hiroshi Takeda Reviewer, Office of New Drug III, PMDA 1 Disclaimer The

More information