Upcoming events / Executive Training
  • September

    19

    2017

    Marketing Authorisation Outside the ICH Region

  • September

    20

    2017

    PharmaFORUM Webcast International

  • September

    25

    2017

    Masterclass EU QPPV

  • September

    28

    2017

    Regulatory Leaders FORUM

  • September

    28

    2017

    HTA Assessment in Germany, Spain, the UK and the EU

  • October

    09

    2017

    Pharmacovigilance Inspection Readiness

  • October

    17

    2017

    Advanced Pharmacovigilance Writing and Management

  • October

    17

    2017

    CMC Documents: Scientific Writing for Regulatory Submission

  • October

    24

    2017

    Marketing Authorisation in ASIA

  • October

    25

    2017

    Getting Biosimilars on the US Market

  • October

    26

    2017

    PV Requirements in Emerging Markets

  • November

    21

    2017

    Marketing Authorisation for Human Medicines in Latin America

  • November

    22

    2017

    Off-Label Use in Europe

  • November

    27

    2017

    EU Regulatory Affairs Introductory Training Course

  • November

    29

    2017

    Scientific Writing: Abstracts and Posters

  • December

    06

    2017

    The EU Regulatory Affairs Expert

  • December

    07

    2017

    Set up of a Global PV Quality & Compliance System

  • January

    23

    2018

    Toxicology Winter School

Regulatory Leaders FORUM
28-09-2017

Do you have years of regulatory affairs experience and carry great responsibility in regulatory affairs? Then, you should not miss the Regulatory Leaders FORUM, where regulatory affairs experts from the industry and from European authorities will provide you with insights into their daily affairs, including practical case studies.

You will leave the conference with new ideas on how to successfully deal with upcoming challenges such as early access schemes, the inclusion of RWE data in marketing authorisations, digital product information and eSubmission requirements.

Since the requirements for eSubmission and IDMP/SPOR are especially challenging, day two will be completely dedicated to these issues. If these issues are not personal priorities, it is possible to attend only day one.

28 - 29 September 2017 in Berlin