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Seminars

Here you will find the list of our seminars

Specifically tailored in-house workshops
  • Regulatory Compliance - Interface between Production and Regulatory Affairs
    This Workshop is designed for 4 hours and will be carried out in-house based on individual and detailed
    consultation (pdf details)
  • XEVMPD (e)Xtended EudraVigilance Medicinal Product Dictionary –
    Setting up the company-internal project
    This workshop is designed for 8 hours and will be carried out in-house based on individual and detailed consultation (pdf details)

Current seminars
03.07.12 Regulatory Compliance & GMP Compliance (details) Köln
09.05.12 Informa’s Filing Variations 2012 (details) Brussels
19.04.12 Änderungsanzeigen korrekt in der Praxis umsetzen (details) Berlin
07.02.12 Regulatory Affairs-Wissen für Mitarbeiter der Herstellung/QA/QC (details) Bonn
01.02.12 Konferenz Regulatorisches (e)Dokumentenmanagement Pharma
Workshop D - EVMPD – Neue EMA-Guidance: Electronic submission of information on medicinal products (details)		 Berlin


Completed seminars
20.07.11 Aktuelle Herausforderungen und Haftungsfragen der Qualified Person (pdf details) Heidelberg
28.06.11 Informa's Filing Variantions Conference (details) (comments) Berlin
17.05.11 Regulatory Compliance an der Schnittstelle zu QA/QC (pdf details) Bonn
12.04.11 Änderungsanzeigen korrekt in der Praxis umsetzen Köln
15.02.11 Regulatory Affairs-Wissen für Mitarbeiter der Herstellung/QA/QC
(pdf details)		 Bonn
30.11.10 Informa's Filing Variantions Conference (details) London
04.11.10 VET: Dokumenten-, Dossier- & Submissionmanagement
(pdf details)		 Heidelberg
18.08.10 Aktuelle Herausforderungen und Haftungsfragen der Qualified Person (pdf details) Mainz
11.05.10 Regulatory Compliance an der Schnittstelle zu QA/QC Bonn
16.03.10 Änderungsanzeigen korrekt in der Praxis umsetzen Köln
04.02.10 Dokumentenmanagement an der Schnittstelle von Produktion/QA und Zulassung Mannheim
21.01.10 Regulatory Affairs-Wissen für Mitarbeiter der Herstellung/QA/QC Bonn
15.09.09 Product Quality Review kompakt Mannheim
14.09.09 IIR-Fachkonferenz „Regulatory Compliance“ (pdf details) Wien
07.07.09 Änderungsanzeigen korrekt in der Praxis umsetzen Köln
26.05.09 Regulatory Compliance / GMP Compliance
16.09.08 Understanding the impact on the new EMEA filing variations guideline on the industry (pdf details) Brussels
03.06.08 Regulatory Compliance / GMP Compliance
18.02.08 European GMP: Current Issues and Future Developments
“How to Achieve and Ensure Regulatory Compliance”
(pdf details)		 Budapest
30.10.07 Achieving regulatory compliance: How Product Quality Review influences companies (pdf details) Amsterdam
28.06.07 Product Quality Review kompakt Frankfurt / Offenbach