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Bethesda North Marriott Hotel and Conference Center

Feb 11, 2019 7:00 PM - Feb 13, 2019 8:15 PM

5701 Marinelli Road, , North Bethesda, MD 20852 , USA

Regulatory Submissions, Information, and Document Management Forum

Session 9: Track 1: Preparing Regulatory Affairs for the Use of SPOR/IDMP and the Benefits it can Bring

Session Chair(s)

Sarah  Powell, RAC

Sarah Powell, RAC

President

Powell Regulatory Services, United States

This session will review the current status of IDMP implementation in the EU and the impact of SPOR on regulatory teams today, and in the future. The session will also review how effective data information management can provide benefits beyond compliance with regulations.

Learning Objective : At the conclusion of this session, participants should be able to:
  • Explain the SPOR implementation in Europe and the impact on daily activities performed by regulatory staff
  • Apply practical recommendations to current processes and systems to prepare the organization for SPOR requirements in the EU
  • Describe the benefits of IDMP to the business beyond compliance
  • Speaker(s)

    Remco  Munnik

    The Use of SPOR/IDMP and the Impact on Regulatory Affairs and RIM Solutions in the EU

    Remco Munnik

    IRISS Forum, Spain

    President

    Kelly  Hnat

    Preparing for SPOR in Europe: What Are the Latest Developments in the EU Implementation of IDMP and What can You do Now?

    Kelly Hnat

    K2 Consulting/Gens & Associates, United States

    Principal

    Andrea  Herrmann, PharmD

    Turning IDMP into an Data and Information Management Project with Benefits Outside of Compliance

    Andrea Herrmann, PharmD

    Merck Healthcare KGaa, Germany

    Head of Regulatory Compliance & Regulatory Information Management

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