Freek Helsper

Regulatory Affairs at Alfasan Diergeneesmiddelen BV
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Contact Information
us****@****om
(386) 825-5501
Location
Woerden, Utrecht, Netherlands, NL
Languages
  • Dutch Native or bilingual proficiency
  • English Full professional proficiency
  • German Professional working proficiency
  • French Elementary proficiency
  • Italian Elementary proficiency

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Experience

    • Netherlands
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Regulatory Affairs
      • Oct 2020 - Present

    • Netherlands
    • Travel Arrangements
    • Volunteer
      • Nov 2005 - Present

      The SKJ is a non-profit organisation organising summer camps for children in the age of 6 to 12 years. Our goal is to provide children from all backgrounds a holiday, camping in the woods. Since 2005 I am a volunteer for this great organisation. I have been the chair of the organization, as well as a member of several committees. The SKJ is a non-profit organisation organising summer camps for children in the age of 6 to 12 years. Our goal is to provide children from all backgrounds a holiday, camping in the woods. Since 2005 I am a volunteer for this great organisation. I have been the chair of the organization, as well as a member of several committees.

    • Netherlands
    • Pharmaceutical Manufacturing
    • Head of R&D and Regulatory Affairs
      • Feb 2018 - Sep 2020

    • Netherlands
    • Pharmaceutical Manufacturing
    • Head of Regulatory Affairs and QA
      • Sep 2009 - Feb 2018

      Veterinary product development and regulatory affairs. Qualified Person for Pharmacovigilance. Veterinary product development and regulatory affairs. Qualified Person for Pharmacovigilance.

    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Head Of Regulatory Affairs and QA
      • Sep 2009 - Feb 2018

      Veterinary product development and regulatory affairs. Qualified Person for Pharmacovigilance. Veterinary product development and regulatory affairs. Qualified Person for Pharmacovigilance.

    • Netherlands
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Consultant Regulatory Affairs
      • Sep 2002 - Aug 2009

      Human and Veterinary regulatory affairs. Management of MA-dossiers, MR- and DC-procedures for the generic industry. Qualified Person for Pharmacovigilance. Human and Veterinary regulatory affairs. Management of MA-dossiers, MR- and DC-procedures for the generic industry. Qualified Person for Pharmacovigilance.

    • United States
    • Higher Education
    • 100 - 200 Employee
    • Undergraduate research project
      • 1999 - 1999

Education

  • Special Air Services
    PPL(A) pilot license
    2019 - 2021
  • Utrecht University
    PharmD, Pharmaceutics
    1995 - 2002
  • The Ohio State University
    Pharmaceutics
    1999 - 1999
  • Kandinsky College
    Atheneum
    1990 - 1995

Community

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