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5th edition Information Management, Data Quality and IDMP as a Long Term Information Management Project

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

27-29 November 2017
Berlin, Germany


Why You Should Attend

5th edition Information Management, Data Quality and IDMP as a Long Term Information Management Project

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

  • Turn IDMP into long term information management project
  • Realise IDMP benefits outside of compliance
  • Establish good data quality production and maintenance
  • Discuss good practices around structuring unstructured data
  • Manage effective compliance work and IDMP strategy in the uncertainty context
  • 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
    • PAREXEL
    • 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 Partners


    Practical Insights From

    Dr. Andrea Herrmann, MDRA
    Director, Strategy Implementation Leader Biopharma | R&D Strategy and Business Operations
    Merck

    Charlotte Ratcliffe
    Regulatory Information Management, IDMP project
    Grünenthal GmbH

    Quentin Grignet
    IDMP Lead
    GSK Vaccines

    Guido Claes
    Director MDM for Pharma R&D
    Janssen Pharmaceutical Companies of Johnson and Johnson

    Dr. Andrew Marr
    Internationally recognised IDMP Compliance Expert Member, ISO TC 215, WG 6
    Marr Consultancy Ltd, UK

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

    Dr. Joerg Stueben
    Senior Expert in Global Regulatory Operations
    Boehringer Ingelheim Pharma GmbH & Co KG

    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
    Latest Conference News & Resources



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    Event Contact

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

    Melini Hadjitheori


    PO Box 24797
    CY-1304 Nicosia


    Telephone:
    +357 22 849 308
    Fax: +357 22 849 394
    Email: MeliniH@marcusevanscy.com