marcus evans europe conferences

Quality Risk Management & Process Validation in the Product Life Cycle

Link the science and quality risk-based approach to the global quality system, monitor continuously quality and data integrity to stay compliant and consistently deliver required quality

28-30 September 2016
Novotel Berlin-Tiergarten, Germany

Why You Should Attend

Quality Risk Management & Process Validation in the Product Life Cycle

This marcus evans conference will help delegates implementing a quality risk management approach into their existing quality systems, understanding how to assess and evaluate risks in their companies and with their Third party partners. They will also gain insights from various companies with the development of continuous process verification, approaching the management of data and preventing potential pitfalls in its implementation.

Pharmaceutical Quality system had shifted in recent years from a traditional model to a more global, dynamic and risk-based approach, enhanced especially by regulatory authorities and economic environment.

The integration of quality risk management is not anymore an option for pharmaceutical companies, which need to improve and strengthen the robustness of their process along the life cycle of their products to facilitate innovation, improvement and compliance. Effective quality system is also guaranteed by continual verification of the data, processes and products, which also need to be implemented within the global quality architecture.

Key Topics

  • Discuss regulatory expectation on quality compliance approaches
  • Define an efficient QRM system and tools across global quality system
  • Design efficient process to assure quality control
  • Correctly handle third-party within QRM processes
  • Apply efficient continuous process verification to monitor the system
  • Previous Attendees Include

    -Eli Lilly
    -Hoffmann-La Roche
    -Novartis Pharma
    -Boehringer Ingelheim
    -Novo Nordisk
    -Johnson & Johnson
    -Bayer Healthcare
    -Bristol-Myers Squibb
    -Daiichi Sankyo
    -Biogen Idec
    -Janssen Pharmaceutical

    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
    Visit website >>

    Event Partners

    Practical Insights From

    Patrick Jonvel
    Global Head Quality

    Andreas Schreiner
    Manufacturing Science and Technology (MS&T) Site Validation Head

    Michael Schousboe
    Principal Specialist Quality Risk Management
    Novo Nordisk

    Manuela Gottschall
    Head Global Quality Risk Management

    Laurence Plapied
    Head of Process Validation (LE) Global Engineering
    Baxalta Belgium.Manufacturing SA

    Mara Ernst
    Drug Safety
    B.A.H. Bonn

    Morten Allesų
    Senior Consultant, Process Technology Consulting, PhD Pharm
    NNE Pharmaplan

    Patrick Enderli
    Head Quality Assurance, AQA
    Arena Pharmaceuticals GmbH

    Click Here For Full Agenda

    Voice of Our Customers
    • “Great. Enjoyed networking” Eisai
    • “Great gathering of professionals in the alliance management” UCB
    • “Overall very good” Merck
    • “Very well organized” Sanofi
    Latest Conference News & Resources

    Join the Discussion

    Follow on LinkedIn

    Event Contact

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

    Yiota Andreou

    marcus evans (Europe) Ltd
    PO Box 24797

    +357 22 849 404
    Fax: +357 22 849 310