CONFERENCE PROGRAMME D R I V I N G Success ACDM Annual Conference 2010

Similar documents
What is Clinical Data Management

Clinical Data Management BPaaS Approach HCL Technologies

Clinical Data Management is involved in all aspects of processing the clinical data, working with a range of computer applications / database systems

Udo Siegmann member of e3c, CDISC Sen. Dir. Acc. Management PAREXEL

Integrated Clinical Data with Oracle Life Sciences Applications. An Oracle White Paper October 2006

UTILIZING CDISC STANDARDS TO DRIVE EFFICIENCIES WITH OPENCLINICA Mark Wheeldon CEO, Formedix Boston June 21, 2013

Professional Developments in Clinical Data Management: The Changing Role of the Data Manager

BIOCLINICA, INC. TO DEMONSTRATE TECHNOLOGY-ENHANCED CAPABILITIES AT UPCOMING GLOBAL INDUSTRY EVENTS

The Evolution of Data Management Job Models. in the Execution of Clinical Trials.

eclinical Services Predictable Pricing Full Service EDC Phase I-IV Sophisticated Edit Checks Drug Supply Chain Forms Library Data Collection Services

KCR Data Management: Designed for Full Data Transparency

Bringing Order to Your Clinical Data Making it Manageable and Meaningful

Clinical Data Management Overview

SAS Drug Development User Connections Conference 23-24Jan08

Opportunities. Sponsorship and Exhibition. 1-2 December 2015 Hilton Birmingham Metropole CNO Summit2015 DB media pack.indd 1 30/09/ :20

Needs, Providing Solutions

Full-Service EDC as an Alternative to Outsourcing

Streamlining the Flow of Clinical Trial Data: EHR to EDC to Sponsor

Rationale and vision for E2E data standards: the need for a MDR

August

TEMPLATE DATA MANAGEMENT PLAN

Avg cost of a complex trial $100mn. Avg cost per patient for a Phase III Study

4. Executive Summary of Part 1 FDA Overview of Current Environment

The Dynamics of DATA MANAGEMENT

Sponsorship & Marketing Opportunities

Welcome and introductions Campbell Keir, Director, Energy and UK Infrastructure, UK Trade & Investment

The Top 10 Contract Research Organizations

Clinical Trial Management Systems (CTMS) - Global Strategic Business Report

UACES 35th Annual Conference and 10th Research Conference The European Union: Past and Future Enlargements. Zagreb, Croatia, 5-7 September 2005

Truly expensive and time consuming?

Programme Guide PGDCDM

In-depth analysis of the report is based on propriety databases, primary and secondary research and inhouse analysis by a team of experts.

Imaging Core Lab Solutions Electronic Data Capture Clinical Trial Supply Planning IWR/IVRS

Bridging Clinical Trial Innovation and Quality

Professional Selling Skills The Psychology of Sales Strategic Selling

To know more about Pharmacovigilance and Clinical Trials Data Management

Remote services are changing your industry. World-class Remote Services Managing Remote Services in the IoT. Are you prepared for the ride?

Our Vision. 2 For complete details and availability contact: or dlafont@the-aaa.org

We are pleased to share the recent topics on CDISC standards with you at the Japan Interchange.

When being a good lawyer is not enough: Understanding how In-house lawyers really create value

AGENDA. Wednesday. Keynote Address: The Evolution of the Pharmacovigilance System Speaker: Dr. David J Lewis, Novartis Pharmaceuticals

Introducing our Chair for the Forum...

Healthcare Link User's Guide

Electronic Submission of Regulatory Information, and Creating an Electronic Platform for Enhanced Information Management

E-Learning Courses. Course Category

Clinical Data Management at Kendle

WEDDINGS AT THE ELYSIUM

End-to-End E-Clinical Coverage with Oracle Health Sciences InForm GTM

BioWorld s PARTNER in FOCUS: Covance AN ADVERTISING SERVICE FROM BIOWORLD

Global Market Study on E-clinical Solution Software: Asia to Witness Highest Growth by 2020

Overview of the CDISC Operational Data Model for Clinical Data Acquisition and Archive (based on CDISC DTD 1.1 Final)

Overview of CDISC Implementation at PMDA. Yuki Ando Senior Scientist for Biostatistics Pharmaceuticals and Medical Devices Agency (PMDA)

Professional Managers Annual Conference Adding value to business schools Programme

Medical Data Review and Exploratory Data Analysis using Data Visualization

Transforming CliniCal Trials: The ability to aggregate and Visualize Data Efficiently to make impactful Decisions

Data Collection Database options and Data Management considerations. Paul Donnelly George Clinical The George Institute for Global Health

PANAGORA PHARMA CUSTOMER EXPERIENCE SUMMIT 14

Data Management: Good Team Work is de sleutel tot succes!

2015 / 2016 Awards Criteria and Submission Information

Sponsorship Opportunities

The 2nd Annual Middle East & North Africa Spectrum Management Conference

A white paper. Data Management Strategies

Featuring case studies and insights from the industry s leading firms and thinkers. operationalizing Data Science in Insurance novarica and Chubb

Careers Advisers Day 16 September Internal Use Only - Not to be disclosed outside Standard Life group

Job Profile Clinical Research Associate III (CRA)

Information for Summit sponsors.

cro s - focus on laboratories

Workshop on Capacity Building of Ethics Committees for Clinical Research in India 08 April 2015, PIMS, Puducherry

Final Guidance on Electronic Source Data in Clinical Investigations Promoting esource Data Capture

datalabs edc REvolutionizing clinical data management

The Institutes Management Education

Blockbuster!!! Content Management in the Pharmaceutical Industry An Overview. Global Pharma Market Shares by Sales (Approx. USD 700 Billion) Global

Agenda General Sessions Breakout Tracks Networking Events June Manchester, UK The Lowry Hotel

THE BIOTECH & PHARMACEUTICAL INDUSTRY

Integrating EHR and EDC systems

Event Sponsorship Opportunities

EFPIA position on Clinical Trials Regulation trialogue

We set things in motion and keep them moving. Metronomia Clinical Research Services

Understanding the links between employer branding and total reward

What We Are..!

Section 1 Project Management, Project Communication/Process Design, Mgmt, Documentation, Definition & Scope /CRO-Sponsor Partnership

Did you know? Accenture can deliver business outcome-focused results for your life sciences research & development organization like these:

Transcription:

CONFERENCE PROGRAMME PHOTO: MARK MCARDLE, CANADA DRIVING Whittlebury Hall Hotel, Northamptonshire 21st-23rd March

DAY 1 09:00 Welcome Speech Tracy Fells, Head of Data Management Operations (Europe), CMED and ACDM Chair, Gail Kniveton, Director BD and Data Services, i3 Pharma Resourcing & Sharon Torpey, Business Coach, Liberty Introduction: Driving. Do you feel like you are in the passenger seat or worse the back seat when it comes to clinical data management and your career? During the conference consider the changes that we face to develop our industry and think what does this mean for me? By the end of the conference you will understand the challenges that we face, have heard potential solutions and are ready to take back and implement new ideas at your own company. Session Chair: Tracy Fells, Head of Data Management Operations (Europe), CMED 09:15 Guest Speaker Diane Jorkasky Chief Medical Officer & SVP, Head of Development, Aileronix Driving for but are we driving as smart as we can? The pharmaceutical business is under huge pressure and needs to be more competitive if it is going to stay successful. Every day companies generate large amounts of data, much of which is never fully leveraged. Traditional approaches to data collection and management prevent the full curation of all data within a company, leading to a substantial opportunity lost for that company. Why is this? Do companies really understand the full power of the data they own? What can be done by members of this organisation to advance the thinking and technology? 10:00 Adapt to Succeed: An Optimal Route to Market Dr Steven Julious, Sheffield University Why are adaptive trials so important to driving success in clinical trials? This presentation will cover trial design from a statistical point of view. 10:45 Coffee 11:00 Oncology Session Breakout Sessions Senior Forum 11:00-12.45 11:00-15:30 11:00-15:30 10:00-12:45 Main Room Breakout Room 1 Breakout Room 2 Breakout Room 3 Oncology (Session details right) EDC Vendor Demo Oracle EDC Vendor Demos Breakout Senior Forum Karen Smith, Associate Director, Business Transformation, Kendle Managing and Enhancing Key Business Partnerships to Drive ful Relationships Session Chair: Fred Daniels, Director, Data Management Premier Research

11:00 Overview of the Various Types of Data that Data Managers Working in Oncology Handle and the Associated Challenges Mary Boyle, Manager, Clinical Data Scientist, GSK This presentation will provide an overview of the various types of data that data managers working in Oncology handle. This will include the challenges Oncology studies present around complex data types such as Lesion and Response, Liver Events, managing multiple AEs / SAEs. 11:20 RECIST Response Evaluation Criteria in Solid Tumours Declan McGuirk, Principal Clinical Data Scientist, GSK This presentation will look at RECIST in more detail. RECIST Response Evaluation Criteria in Solid Tumours. What it is and why it is important in Oncology? 11:40 Overcoming Data Management Operational Challenges in Oncology Studies Trevor Griffiths, Senior Manager, Data Management, i3 Statprobe This presentation will discuss overcoming data management operational challenges in oncology studies, from a CRO perspective. 12:00 Integrating a ful Oncology Document Management System Mukhtar Ahmed, VP Consulting and Partners, Medidata Solutions Oncology Data Management requirements play a vital role in the accurate, timely, and thorough information that contributes to the success of clinical studies and cancer research. This session will share the steps and techniques that are required for a successful integrated Oncology Data Management system. 12:20 Early Phase Oncology Requirements Becky Hogg, Team Manager, DMO, CMED This presentation will cover early phase oncology requirements. This includes how to manage complicated protocols, including adaptive designs. Also how to capture non ecrf data, in all it s guises! 12:40 Oncology Panel Discussion 12:45 Lunch 14:00 ACDM AGM Session Chair: Sue Gales, Associate Director of Data Management, Pfizer 14:45 Dictionaries, Dictionaries Everywhere... Ian Slack, World Wide Coding Consultant, Parexel and ACDM coding SIG Lead This presentation will aim to answer all the questions you ve wanted to know but were afraid (or didn t know) to ask! 15:10 To Train or not to Train...? Jacqueline Johnson, Training Consultant and ACDM training committee leader, Dovetail Training and Gail Kniveton, Director BD and Data Services, i3 Pharma Resourcing This presentation will help you to understand how to choose training that s right for you and your team. 15:30 Coffee

16:00 Driving Data Management the Cost, Future and Unknown Breakout Sessions Main Room (Session details below) Breakout Room 1 Personal Development Session Sharon Torpey, Management Coach, Liberty What can you do get back into the driving seat for your career and personal development? Breakout Room 2 Project Management Special Interest Group Session Kjell Pennert Director Data Management, Richmond Pharmacology Driving success with highly effective project management Breakout Room 3 EDC Special Interest Group Session Chris Barden, CRF Health Driving success with EDC Session Chair: Vivienne Yeap, Study Data Manager, Clinical Data Management, Roche 16:00 Analysis of metrics related to quality, time, and cost for EDC trials John Griffiths, Manager, Database Programming, Pharmanet This presentation will consider EDC metrics. As the percentage of EDC trials continues to grow at a fast pace, it becomes increasingly important to collect and analyse metrics related to quality, time, and cost for EDC trials. 16:20 Future of epro Valdo Arnera, General Manager, Europe, PHT This presentation will describe what seems to be the future of epro, with the probable increasing use of the web and mobile phones as well as the point of view of the regulatory bodies in the US in Europe and in Japan, based on several interactions with various agencies. 16.40 Its Phase 1 Data Management but not as you know it Rachel Darby-Dowman, Cancer Research UK Its Phase 1 Data Management but not as you know it Data Management in the not for profit sector. This talk will discuss oncology trials in the academic and not for profit sector. 17:00 Day 1 round up Tracy Fells, Head of Data Management Operations (Europe), CMED and Gail Kniveton, Director BD and Data Services, i3 Pharma Resourcing 19:00 Champagne Reception 19:30 Gala Dinner If you have any questions or would like to exhibit please contact us by Email admin@acdm.org.uk or by telephone 01727 896080.

DAY 2 09:30 Welcome Speech Tracy Fells, Head of Data Management Operations (Europe), CMED and Gail Kniveton, Director BD and Data Services, i3 Pharma Resourcing 09:35 The debate Julianne Hull, Senior Director, Global Development Data Operations, Pfizer This house believes that regulatory inspections don t drive success Other expert debaters to be confirmed 10:30 Coffee Sponsored by Richmond Pharmacology Session Title: Lab and Other External Data Session Chair: Vicky Wiggins, Project Manager, i3 Statprobe 11:15 A thorough approach to QT studies Kjell Pennert, Director of Data Management, Richmond Pharmacology This presentation will discuss a semi-automated standardised process from the preparation and calibration of the ECG machine, to reconciliation with the clinical database, reading of the ECG trace, to delivery of data sets for statistical analysis. 11:40 epro Integration Paolo Morelli, CROS NT, Managing Director This presentation will outline how E-PRO has been integrated most effectively with clinical trials databases. 12:05 Realising the benefits of integrating laboratory normal range data with an EDC system Edward Jones, Customer Manager, Phase Forward During this session Ed Jones will review the primary benefits to be gained in data quality and patient safety through the use of tools such as Phase Forward s Lab Normal Ranges Management Tool (LNMT). 12:30 End of Session Panel and Audience Discussion 12:45 Lunch Session Title: Data Standards and Quality Session Chair: Ian Pinto, Project Data Leader, Roche 14:00 Every Patient Every Visit Lewis Watkinson, Associate Director, Program Data (supporting the Primary Care Business Unit), Pfizer Every Patient Every Visit, or EPEV, is a methodology that facilitates the monitoring of real-time data retrieval and cleaning by defining and presenting the status of key components of cleaning through a flexible tracking and metrics producing framework. Find out more about how Pfizer have implemented this to drive success.

14:25 Using eclinical Tools to Improve Data Quality Jonathan Andrus, Vice President Data & Study Operations, BioClinica Data quality in an EDC environment doesn t have to wait until the end of the study: thinking ahead and designing and developing a quality-oriented study is critical. This presentation will provide examples and an overall case study that will help bring the material to life and provide real world best practices. 14:50 Using CDISC ODM to Deliver Proven Time and Cost Savings in Study Set-up Mark Wheeldon, Chief Executive Officer, Formedix This presentation will present three real-life use cases (with real companies) where CDISC ODC has been proven to save time and money during the study set-up process in EDC. 15:15 Finding the right BPO partner Chinnie Nwandu, Clinical Data Management Domain Specialist, Roche This presentation will help you to understand how to identify and address the issues in finding the right BPO partner, with similar corporate values is only the first steps in ensuring a successful off-shore partnership in India. 15:40 Coffee Session Title: The Future of Data Management Session Chair: Sharon Torpey, Business Coach, Liberty 15:50 What will data management look like in 2015? What can we do to prepare? Linda Talley, Lilly and Richard Young, Medidata Solutions leading the INCDMA (International Clinical Data Management Associations) Team This is an interactive panel discussion to conclude the conference to get everyone discussing what data management will look like in 2015 and what we can do to prepare. Please bring your ideas and discussions for this event. 16:40 Day 2 round up and close ACDM Board How to Book To register on-line for the ACDM Annual Conference visit our website www.acdm.org.uk. If you have any questions or would like to exhibit please contact us by Email admin@acdm.org.uk or by telephone 01727 896080.