• Company
• Industries
• Consulting
• Project Management
• GXP
• Training
• Information

• Events 2024
• Events 2023
• Events 2022
• Events 2021
• Events 2020
• Events 2019
• Events 2018
• Events 2017
• Events 2016
• Events 2015
• Events 2014
• Events 2013
• Events 2012
• Events 2011
• Events 2010
• Events 2009
• Events 2008

Events 2012

• 13. - 14.03.2012
  Berlin: 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
  
• 15. - 16.03.2012
  Vienna: Handling Changes and Variations
  In this two days conference, Dr. Hiltrud Horn will give presentations on how to deal with manufacturing process changes and with packaging changes. Furthermore, detailed insight will be provided on ... More
  
• 09. - 10.05.2012
  Brussels: Filing Variations 2012
  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
  
• 22. - 23.05.2012
  Cologne: Der Regulatory Affairs Manager
  During this two days seminar, Dr. Hiltrud Horn will give detailed insight into the essentials of Regulatory Affairs. You will learn how to prepare the Quality part of the dossier and how to deal with ... More
  
• 19. - 21.06.2012
  Munich: 8th Bio Production Forum
  In this three days conference, Dr. Hiltrud Horn will show you what is really important for the development of biotech products. You will learn how to deal with GMP and regulatory aspects. For more ... More
  
• 26. - 28.06.2012
  Heidelberg: Der GMP-Beauftrage in der Biotechnologie
  In this three days conference, Dr. Hiltrud Horn will give detailed insight in the Process Transfer from Development to Commercial Manufacturing with a case study. Her presentation will cover the ... More
  
• 12. - 13.09.2012
  Prague: GMP-compliant Process Transfer
  In this conference, Dr. Hiltrud Horn will show how to develop a regulatory strategy for a site change covering EU and US. Furthermore Dr. Horn will present how to handle changes during a process ... More
  
• 18.09.2012
  Cologne: Regulatorische Anforderungen an Primärpackmittel
  In this conference, Dr. Hiltrud Horn will give detailed insight in the regulatory aspects for primary packaging material. Furthermore Dr. Horn will present how to address the information on packaging ... More
  
• 02.10.2012
  Mannheim: FDA kompakt: Organisation, Systeme, Compliance
  In this conference, 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 Dr. Horn will ... More
  
• 10. - 12.10.2012
  Heidelberg: GMP Compliance for Biopharmaceuticals and ATMP
  During this three days seminar, the attendees will learn important GMP- and regulatory aspects of the development of biopharmaceuticals and ATMPs. Dr. H. Horn will give several presentations ... More
  
• 18. - 19 .10.2012
  Frankfurt: IMPD & CTA für Biotech-Arzneimittel
  On October 19, 2012, Dr. Hiltrud Horn will present the essentials of clinical trials and will give you practical advice on the Dos and Don'ts.   For more information please visit the following ... More
  
• 08. - 09.11.2012
  Frankfurt: 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 ... More
  
• 13. - 14.11.2012
  Vienna: How to write the Quality Part of an IMPD
  In this two days conference, Dr. Hiltrud Horn will give detailed insight into the Quality Part of an IMPD. Her presentations on the first day will cover regulatory requirements and challenges of the ... More
  
• 14. - 15.11.2012
  Mannheim: Pharmaeinkauf und GMP compliance
  In this two days conference, Dr. Hiltrud Horn will focus on important GMP-aspects for supply change management. Furthermore she will explain how to deal with changes of suppliers and how to stay ... More
  
• 27. - 28.11.2012
  Barcelona: Stability Testing for Drug Substances and Drug Products
  On November 27 and 28, 2012, Dr. Hiltrud Horn will provide you with essential hints on how to write the stability section of the CTD for drug substances and drug products. Furthermore, she will talk ... More
  
• 04. - 05.12.2012
  Mannheim: Single-Use Disposables
  In this conference Dr. Hiltrud Horn will talk about regulatory aspects for the development of biotech products in EU and US and will also cover specifics of single-use equipment. For more ... More