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Overview

Note: This Forum builds upon and replaces previous DIA eDM and IDMP conferences.

First there was the steam engine, then the telephone, and now we stand in the midst of the next revolution as we address “the internet of things.” This instant information exchange affects not only the abundance of data and formats of information sharing, but also affects our role as drug and device developers as we explore processes that don’t require human intervention.

eDM 2018 - Clinical and Regulatory Operations Forum focuses on how we can adapt to this new data revolution by embracing working solutions and partnerships. This highly interactive forum will enable you to perform complex tasks to the highest operational standards to shorten turnaround times and reduce queries and re-creation in your development programmes.

We are bringing together thought leaders across the fields of:

• Clinical Operations
• Records and Document Management
• Regulatory Affairs
• Health Authorities
• Supportive software vendors
• CROs

The meeting will be based on selected abstracts that showcase working solutions and will allow attendees to learn from implemented best practices.

Submit an Abstract

Become an active part of the forum you attend by holding a presentation. Submit an abstract and take this opportunity to present your research and work to your peers at the conference. It’s the perfect place for you to put your research into the limelight, to create a discussion around your result with other professionals or to generate interest around a subject you feel needs more attention.

Learn more on how to submit an abstract here.

Featured topics

• Clinical Operations
• Records and Document Management
• Regulatory Affairs
• Health Authorities
• Supportive software vendors
• CROs

Who should attend?

  • Health Care- and R&D Professionals in the areas of Electronic Document Management, IT and Process Innovation
  • Clinical Operations and Regulatory Affairs that want to excel in their day-to-day work
  • R&D Quality Leads, as well as Trial Managers and Drug Programme Leads & Clinical and Regulatory Project Managers that need to get an overview of the latest gold standards in R&D Operational Excellence to set the standards for high-performing cross functional drug development teams
  • New Technical Solution Vendors

Program Committee

  • Romuald  Braun, MSc
    Romuald Braun, MSc Vice President, Strategy - Life Sciences
    AMPLEXOR, United States
  • Hans  van Bruggen, MSc
    Hans van Bruggen, MSc Regulatory Affairs Scientist
    eCTDconsultancy B.V., Netherlands
  • Karen Jane Roy, MPharm
    Karen Jane Roy, MPharm Senior Vice President, Client Solutions
    Phlexglobal, United Kingdom
  • Eldin  Rammell
    Eldin Rammell Managing Director & Principal Consultant
    Rammell Consulting Ltd, United Kingdom
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Digital Learning Catalog

DIA Learning: 2018 eLearning Soultions
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