Freek Helsper
Regulatory Affairs at Alfasan Diergeneesmiddelen BV- Claim this Profile
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Dutch Native or bilingual proficiency
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English Full professional proficiency
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German Professional working proficiency
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French Elementary proficiency
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Italian Elementary proficiency
Topline Score
Bio
Experience
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Alfasan Diergeneesmiddelen BV
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Netherlands
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Regulatory Affairs
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Oct 2020 - Present
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SKJ Nijmegen
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Netherlands
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Travel Arrangements
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Volunteer
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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.
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Curados B.V.
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Netherlands
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Pharmaceutical Manufacturing
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Head of R&D and Regulatory Affairs
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Feb 2018 - Sep 2020
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Le Vet. Pharma
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Netherlands
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Pharmaceutical Manufacturing
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Head of Regulatory Affairs and QA
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Sep 2009 - Feb 2018
Veterinary product development and regulatory affairs. Qualified Person for Pharmacovigilance. Veterinary product development and regulatory affairs. Qualified Person for Pharmacovigilance.
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AST Farma
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Head Of Regulatory Affairs and QA
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Sep 2009 - Feb 2018
Veterinary product development and regulatory affairs. Qualified Person for Pharmacovigilance. Veterinary product development and regulatory affairs. Qualified Person for Pharmacovigilance.
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DADA Consultancy B.V.
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Netherlands
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Consultant Regulatory Affairs
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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.
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The Ohio State University College of Pharmacy
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United States
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Higher Education
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100 - 200 Employee
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Undergraduate research project
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1999 - 1999
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Education
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Special Air Services
PPL(A) pilot license -
Utrecht University
PharmD, Pharmaceutics -
The Ohio State University
Pharmaceutics -
Kandinsky College
Atheneum