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Hotel Pullman Brussels Midi

2016年6月06日 (月) 午前 9:00 - 2016年6月06日 (月) 午後 5:00

Place Victor Horta 1, 1060 Brussels, Belgium

DIA-TOPRA Workshop on Falsified Medicines

This conference will take stock of where we stand in the EU on falsified medicines and paint the landscape of the global issue. The speakers will present the approaches of the Member States on the implementation of the new legislation, and the impact and achievements of the concerned stakeholders such as industry, patients, pharmacies and distributors who have worked independently and together to find solutions.

概要

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This conference will take stock of where we stand in the EU on falsified medicines and paint the landscape of the global issue. The speakers will present the approaches of the Member States on the implementation of the new legislation, and the impact and achievements of the concerned stakeholders such as industry, patients, pharmacies and distributors who have worked independently and together to find solutions. The key messages of the meeting will be presented in a paper outlining the positive benefits until now and also the challenges yet to be addressed.

Please register for the event at TOPRA website.

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Continuing-Education

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何を学ぶか

  • Understand the nature of the issue at the EU and global level comprehensively
  • Hear from the Member States on their approaches on the endorsement and implementation
  • Discuss how to navigate the various systems and exchange experiences on challenges and solutions
  • Address the challenges linked to the whole supply chain by bringing the stakeholders to the same table and understand the challenges each stakeholder group is addressing

参加対象

The meeting is intended for professionals working with the implementation of the new rules in various points of the supply chain. Regulators or policymakers involved in the endorsement of the rules at national level and professionals participating in the stakeholder groups of manufacturers, market authorisation holders, wholesalers, pharmacy owners and managers and patient representatives would find the meeting interesting as well.

プログラム委員会

  • Ursula Busse, PHD, MBA
    Ursula Busse, PHD, MBA CMC Regulatory Affairs Advisor
    Self employed, France
  • Gerald W. Heddell
    Gerald W. Heddell Director, Inspection Enforcement & Standards Division
    Medicines and Healthcare products Regulatory Agency (MHRA), United Kingdom
  • Susanne Keitel, DRSC, RPH
    Susanne Keitel, DRSC, RPH Director
    European Directorate for the Quality of Medicines & Healthcare (EDQM), France
  • Syed Qadri
    Syed Qadri Lead Consultant
    GENPACT Pharmalink, United Kingdom

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