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 Regulatory Konferenzschwerpunkte im Bereich eDokumentenmanagement

Jan 30 - Feb 1
Berlin, Germany

This is the only conference of its kind in German speaking countries, focused on comprehensive pharma-specific information from the document for information management and archiving.
 
Conference highlights:

  • Will you meet the requirements of the new ISO standard IDMP rapidly meet
  • Listen practice reports linking the regulatory systems Get strategies for long-term archiving and ensuring long term stability data format
  • Find out about the implementation of an enterprise-wide information management forward line with DMS
  • Make use of electronic signatures in accordance with the requirements of 21 CFR Part 11
 
The topics include:

  • Global DMS
  • Electronic signature
  • Submission Management
  • PIM-change
  • Linking regulatory systems
  • Long-term archiving
 
For more information visit http://www.iqpc.com/Event.aspx?id=596388

See you in Berlin!


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