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Lectures

Lectures

 Several event organisers regularly invite our employees to give lectures. Why not visit one of these events and gain an impression of our competence?

  • Hönig J
    Basisseminar Arzneimittelzulassung für Neueinsteiger und Nichtzulasser
    [Basic seminar "Marketing authorisation" for newcomers and people with non regulatory affairs background]
    APV
    28.-29.11.2010, Frankfurt
  • Ahlert J, Hönig J
    Qualitätsgutachten & Dokumentationen im CTD-Format
    [Quality assessment & documentation in CTD format]
    FORUM
    06.-08.03.2012, Bonn
  • Dobmeyer T, Möller J
     English writing and reviewing in regulatory affairs
     FORUM 18.04.2012, Frankfurt
     
  • Tolkmitt F
    Drug Delivery Devices
    APV
    23./24.11.2011, Berlin

  • Dobmeyer T.
    Arzneimittelsicherheit - Status quo 2011 und Ausblick -
    [Drug safety - status quo in 2011 and outlook -]
    BAH-WIDI
    17.11.2011, Bonn

  • Ahlert J, Hoffmann V
     Das generische Zulassungsdossier
    [The generic marketing authorisation dossier]
     FORUM 06.10.2011, Frankfurt

  • Hönig J
    Basisseminar Arzneimittelzulassung für Neueinsteiger und Nichtzulasser
    [Basic seminar "Marketing authorisation" for newcomers and people with non regulatory affairs background]
    APV
    27./28.09.2011, Frankfurt
  • Hönig J, Troost R
    Good Regulatory Compliance & SOPs in Regulatory Affairs
    FORUM 13./14.07.2011, Frankfurt
  • Zimmer M
    Generische Zulassung - Daten, Verfahren & Rechtsfragen
    [Generic marketing authorisation in EU & USA]
    FORUM 30.06./01.07.2011, Bonn

  • Hoffmann V
     Regulatory Affiars für Nicht-Zulasser
    [Regulatory affairs for people with non-regulatory affairs background]
     FORUM 07.06.2011, Frankfurt

  • Tolkmitt F
    Auf einen Blick: Aktuelle Normen und Vorgaben für Medizinprodukte
    [At a glance: Current standards and guidelines for medical devices]
    APV 19.05.2011, Frankfurt

  • Hoffmann V
     European Regulatory Procedures for Medical Writers 
     32th EMWA Conference
     EMWA
     13.05.2011, Berlin

  • Tolkmitt F
    Genehmigung von Klinischen Prüfungen bei Medizinprodukten
    [Approval of clinical trials for medical devices]
    FORUM 12.04.2011, Frankfurt
  • Troost R, Zimmer M
    Generika - Lizenzierung, Kauf, Vertragsgestaltung
    [Generic products - licensing, purchase, drafting of contracts]]
    FORUM 05.04.2011, Offenbach

  • Tolkmitt F
     2nd European Annual Conference on Clinical Trial Supplies
     Increasing efficiency in the Clinical Trial Supply Chain
     APV
     05.04.2011, Kassel

  • Martini C
    Das europäische Zulassungssystem für Arzneimittel - ausgewählte Themen
    [The European marketing authorisation system for medicinal products – selected topics]
    BAH-WIDI
    23.03.2011, Bonn

  • Hönig J
    Das Europäische Zulassungsystem für Arzneimittel – Grundlagen
    [The European marketing authorisation system for medicinal products – fundamentals]
    BAH-WIDI
    22.03.2011, Bonn
  • Ahlert J
    CTD: Qualitätsgutachten & Dokumentation
    [CTD: Quality assessment & documentation]
    FORUM16.03.2011, Köln

Please note:

We also organise in-house seminars. (In accordance with our customers' wishes we have decided not to list these seminars here.) However, perhaps you are interested in inviting us to stage seminars on specific subject areas on your company premises.

Your quick link to all the subject areas:

Company

Medicinal products

Medical devices