ユーザーIDをお忘れですか? or パスワードをお忘れですか?

メニュー 戻る Short-Courses

How to Register

Register Online for DIA Europe 2018


Register Online
Pay with Credit Card
or by Invoice

Registration Questions


09:00AM – 05:30PM


Send Email

Preconference Short Courses

Held on April 16 & 17, DIA Europe 2018 hosts courses to enhance your meeting experience and maximise your time in Basel.

Short Courses require separate registration. Please click the "Learn More" button under each course to see more details and to register.

  • Workshop: Revision of the EU Clinical Trial Risk Mitigation Guideline

    Monday, 16 April, 14:00 - 17:30

    Jan Willem Van der Laan
    Section on Pharmacology, Toxicology and Kinetics (FTK), Medicines Evaluation Board (MEB), Netherlands

    David Jones
    Expert Pharmacotoxicologist, Clinical Trials Unit, Medicines and Healthcare products Regulatory Agency (MHRA), UK

  • Hot Topics in Pharmacovigilance

    Monday, 16 April, 14:00 - 17:30

    Anja Van Haren
    EudraVigilance Coordinator, Medicines Evaluation Board (MEB), Netherlands

    EMA Instructor Invited

  • Moving from Risk Management to Benefit-Risk Management – Embedding Pharmacovigilance Principles into the Product Life Cycle

    Monday, 16 April, 14:00 - 17:30

    Shelley Gandhi
    Director Pharmacovigilance and Drug Safety, NDA Group, UK

  • The Science of Lay Language Communication Applied in a Pharmaceutical Context: Readability and Understanding of Documents

    Tuesday, 17 April, 09:00 - 12:30

    Thomas M. Schindler
    Head Medical Writing Europe, Boehringer-Ingelheim Pharma GmbH, Germany

    Claudia Thoms
    Institute of Communication Science and Theory of Communication, University of Hohenheim, Germany

    Oliver Haug
    Managing Director, H&H Communication Lab GmbH – The Readability Resource, Germany

  • Genomics in Clinical Development

    Monday, 16 April, 14:00 - 17:30

    Thomas Szucs
    ECPM, University of Basel and Helsana Health Insurance, Switzerland

    Urs Meyer
    Biocenter, University of Basel, Switzerland

  • Current Medical Device Market Surveillance and Vigilance Reporting Requirements in Europe - Concept and Best Practices

    Tuesday, 17 April, 09:00 - 12:30

    Course details to be confirmed.

  • Guidance for Patient Involvement in Pharmaceutical Industry-Led Research

    Monday, 16 April, 14:00 - 17:30