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5th Edition Regulatory Information Management and Data Quality for Pharma Sector

Working towards effective information management and data as an asset vision with tangible business benefits while breaking silos between divisions

12-13 April 2018
Sofitel Kurfürstendamm, Berlin, Germany

Why You Should Attend

5th Edition Regulatory Information Management and Data Quality for Pharma Sector

This marcus evans conference will focus on gathering corporate professionals from Regulatory Operations, Regulatory Affairs, Master Data Management, Regulatory Information Systems and other key stakeholder departments progressing on IDMP projects in the uncertainty context with already some lessons learnt and practices to share for those who are less advanced in the journey.

Join this practitioner IDMP knowledge exchange platform to discuss latest regulatory developments from EMA, FDA developments on GINAS and hear a number of case studies on IDMP projects, technology selection, preparations for the first iteration, practical experiences on unstructured information and other key areas compliance requirements preparations.

Key Topics

  • Boehringer Ingelheim International GmbH leveraging EMA´s new organisations system OMS
  • GSK Vaccines sharing good practices on benefits outside of compliance
  • Johnson & Johnson Consumer Services EAME Ltd. UK breaking the silos between the business and IT teams
  • Merck KGaA focusing on long term information management project
  • Previous Attendees Include

    • Abbott Laboratories GmbH
    • Allergopharma GmbH & Co. KG
    • ArisGlobal GmbH
    • Bayer Pharma AG
    • Boehringer Ingelheim Pharma GmbH & Co
    • F.Hoffmann-La Roche Ltd
    • Fresenius Kabi Deutschland GmbH
    • HighPoint Solutions LLC
    • Janssen Pharmaceutical
    • Johnson & Johnson
    • Oracle
    • Orion Pharma
    • Pfizer Incorporated
    • Pierre Fabre Laboratories
    • Roche
    • Sanofi Pasteur MSD
    • Takeda Pharma A/S ∙ Teelia EU
    • Teva Pharmaceuticals
    • UCB Biopharma SPRL

    Why Choose marcus evans?

    marcus evans specialises in the research and development of strategic events for senior business executives. From our international network of 63 offices, marcus evans produces over 1000 event days a year on strategic issues in corporate finance, telecommunications, technology, health, transportation, capital markets, human resources and business improvement.

    Above all, marcus evans provides clients with business information and knowledge which enables them to sustain a valuable competitive advantage and makes a positive contribution to their success.

    Event Sponsors
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    Event Partners

    Practical Insights From

    Dr. Andrea Herrmann, MDRA
    Head of IDMP Office – GRA Operations Biopharma | Global Regulatory Affairs & RDQ

    Charlotte Ratcliffe
    Regulatory Information Management, IDMP project
    Grünenthal GmbH

    Georg Zimmer
    Manager Data Improvement | Quality Analytics | Bioresearch Quality & Compliance
    Janssen-Cilag GmbH

    Quentin Grignet
    IDMP Lead
    GSK Vaccines

    Sheila Elz
    RA Master Data Manager
    Bayer AG

    Christopher Dunn
    IDMP Systems Lead
    Johnson & Johnson Consumer Services EAME Ltd. UK

    Dr. Joerg Stueben
    Head of Regulatory Information Management and Senior Expert
    Boehringer Ingelheim International GmbH

    Click Here For Full Agenda

    Voice of Our Customers
    • “Very fruitful conference, excellent presenters. Thank you.” IDMP Project Lead, Novartis Pharma AG
    • “Great job!” Research Director, Gartner
    • “Very targeted and productive event. Topic is timely and current.” VP, Life Sciences R&D Practice, HighPoint Solutions
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    Event Contact

    For all enquiries regarding speaking, sponsoring and attending this conference contact:

    Melini Hadjitheori

    Demostheni Severi avenue
    Nicosia, Cyprus

    +1 312 540 6347
    Fax: +357 22 849 380