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Events 2008

• 09. - 10.06.2008
  Prague: The FDA Organisation, Inspection, Application and Approval
  During this two days seminar in Prague, the attendees learnt from Dr. Hiltrud Horn the essentials about regulatory requirements in US and preparation of dossiers in US. Furthermore Dr. Horn presented ... More
  
• 23. - 26.06.2008
  Dublin: Biopharmaceutical Development and Manufacturing
  At this conference, Dr. Hiltrud Horn gave an intensive 1 day training workshop about the regulatory requirements and strategies to be considered for clinical trials, preparation of IMPDs and ... More
  
• 22. - 25.07.2008
  Mannheim: Certified Regulatory Affairs Manager
  On this four days seminar, Dr. Hiltrud Horn gave an intensive three days training course on regulatory requirements in Europe and US. The participants received a detailed insight into all regulatory ... More
  
• 28. - 29.08.2008
  Cologne: Sichere Zulassung bei der FDA
  Dr. Hiltrud Horn gave a two day intensive training in Köln about regulatory requirements in US. On this event, Dr. Horn gave detailed insight into the FDA regulated world. People learnt how to ... More
  
• 16. - 17.09.2008
  Brussels: Filing Variations 2008
  In this two days conference, Dr. Hiltrud Horn gave a presentation on how to deal with change control within a global company. (Conference organized by Informa) More
  
• 23. - 26.09.2008
  Düsseldorf: Certified Regulatory Affairs Manager
  On this four days seminar, Dr. Hiltrud Horn gave an intensive three days training course on regulatory requirements in Europe and US. The participants received a detailed insight into all regulatory ... More