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Events 2009

• 20. - 23.01.2009
  Heidelberg: Certified Regulatory Affairs Manager
  Dr. Hiltrud Horn will give an intensive training course on regulatory requirements in Europe and US. You will get detailed insight into all regulatory documents to be prepared during all phases of ... More
  
• 27. - 29.01.2009
  Rome: Conference on Investigational Medicinal Products
  On 27 January 2009, Dr. Hiltrud Horn will give a one day- training course on the preparation and submission of IMPDs. Her presentation will cover various aspects of how to compile, organise and ... More
  
• 26. - 27.02.2009
  Prague: Change Control - New Aspects and Best Practices
  If you want to know how to handle changes in US and how to implement a comprehensive change control system within your company, then you should attend the “Change Control – New Aspects and Best ... More
  
• 30.03. - 01.04.2009
  Prague: Development of Biopharmaceuticals - Preclinical and Clinical Phases
  In this Conference, Dr. Hiltrud Horn will cover the topic of “Marketing Authorisation for Biotech Products” on April 1, 09. For more information please visit the following ... More
  
• 08. - 10.06.2009
  Brussels: GMP and GCP Compliance for Investigational Products
  On 8 June 2009, Dr. Hiltrud Horn will give a one day- training course on the “How to successfully plan and start a clinical trial”. Her presentation will focus on the essentials of clinical ... More
  
• 16. - 19.06.2009
  Munich: Biopharmaceutical Development and Manufacturing: Developing Tomorrows Medicines and Technologies –
  On 18 – 19 June 2009, Dr. Hiltrud Horn will give a two day- training course on “Development of Biotech Products and Advanced Therapy Medicinal Products (ATMPs) - Regulatory and GMP Aspects -” ... More
  
• 08. - 09.09.2009
  Bonn: MR- & Dezentrales Verfahren
  In this conference, Dr. Hiltrud Horn will give detailed insight in the Mutual Recognition- and Decentralised Procedure including development of strategies and communication with ... More
  
• 23. - 24.09.2009
  Cologne: Projektmanagement in Regulatory Affairs
  During this two days seminar, the attendees will learn important aspects of drug registration (CTD) and project management. Dr. Hiltrud Horn will be one of the main speakers. For more information ... More
  
• 01.10.2009
  Frankfurt: Regulatorische Anforderungen an Primärpackmittel
  In this conference, Dr. Hiltrud Horn will give detailed insight in the regulatory aspects for primary packaging. Furthermore Dr. Horn will present how to address the information on packaging in the ... More
  
• 13. - 16.10.2009
  Berlin: PDA-EMEA Joint Conference 2009 – Ensuring patient safety through supply chain control and GMP
  Dr. Hiltrud Horn will present the “Regulatory Challenges for ATMPs”. Based on her experience on Advanced Therapy Medicinal Products she will give detailed insight in the most important aspects from a ... More
  
• 29. - 30.10.2009
  Mannheim: FDA kompakt: Organisation, Systeme, Compliance
  During this two days seminar, Dr. Hiltrud Horn will give detailed insight into the essentials about regulatory requirements in US and preparation of dossiers in US (IND, NDA, DMF). Furthermore ... More
  
• 01. - 02.12.2009
  London: Filing Variations 2009
  In this two days conference, Dr. Hiltrud Horn will give a presentation on how to deal with change control within a global company.   For more information please visit the following ... More