Ilias G. Zontiros

Senior Regulatory Expert at regenold GmbH
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Contact Information
us****@****om
(386) 825-5501
Location
Badenweiler, Baden-Württemberg, Germany, DE
Languages
  • Czech -
  • Greek -
  • English -

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Eirini Pantoula

Ilias was a valuable partner and his help and guidance was really important during our collaboration in Genepharm S.A. Very professional person and excellent personality.

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Experience

  • regenold GmbH
    • Germany
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Senior Regulatory Expert
      • 2012 - Present

      Procedure Management of National, MRP, DCP and Centralised ProceduresCommunication with Regulatory Health AgenciesParticipation in Scientific Advice MeetingsManagement of preparation of dossiers for submission, procedural workflow and preparation of responsesManagement of lifecycle procedures including variations, PSURs and renewalsRx to OTC Switch strategyStrategic advice to International clients in a variety of projectsCompilation of eCTD dossiers Procedure Management of National, MRP, DCP and Centralised ProceduresCommunication with Regulatory Health AgenciesParticipation in Scientific Advice MeetingsManagement of preparation of dossiers for submission, procedural workflow and preparation of responsesManagement of lifecycle procedures including variations, PSURs and renewalsRx to OTC Switch strategyStrategic advice to International clients in a variety of projectsCompilation of eCTD dossiers

  • Genepharm SA
    • Greece
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Vice President, Regulatory Affairs
      • Feb 2009 - Dec 2011

      MRP/DCP and National Applications Coordination and Strategy for patent expiry productsCommunication with Regulatory Health AgenciesSubmission of dossiers and coordination of procedures for the company’s clientsIdentification of potential development products in co-operation with Research and Development Department as well as with Business Department MRP/DCP and National Applications Coordination and Strategy for patent expiry productsCommunication with Regulatory Health AgenciesSubmission of dossiers and coordination of procedures for the company’s clientsIdentification of potential development products in co-operation with Research and Development Department as well as with Business Department

  • ratiopharm
    • Germany
    • Pharmaceutical Manufacturing
    • 300 - 400 Employee
    • Head of MRP Centre
      • Jul 2004 - Dec 2008

      Head of MRP Centre - procedure management and submissions

    • Regulatory Affairs Manager
      • Dec 2001 - Jun 2004

      Country Manager for UK & IE

Education

  • University of Birmingham
    MSc., Toxicology
    1991 - 1992
  • Ohio University
    BSc, Forensic Chemistry
    1986 - 1991

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