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Diploma
Page Content DIPLOMA IN PHARMACEUTICAL REGULATORY AFFAIRS
To obtain a Diploma in Pharmaceutical Regulatory Affairs, participants must pass eight modules of own choice, including the examinations, within 5 years.
One module from the Medicademy Pharmacovigilance programme may be included in the Medicademy
Regulatory Affairs Diploma.
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Regulatory Affairs |
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Pharmacovigilance |
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Individual Courses |
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E-learning |
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Stine Folkenberg Hedegaard
Stine Folkenberg Hedegaard is E-learning Manager and responsible for e-learning, communication, marketing and a number of courses.
Helle Rishøj Nielsen
Helle Rishøj Nielsen is Payroll Officer and is responsible for payroll, travel arrangements, evaluations, diplomas and certificates, etc.
Minna K. Jørgensen
Minna Kjær Jørgensen is Program Director, Medicademy Pharmacovigilance and also responsible for Introduction to Safety & Pharmacovigilance and Medical Advertising Standards.
Tina Jensen
Tina Jensen is Program Director, Medicademy Regulatory Affairs and responsible for Introduction to Drug Registration.
Henrik Køhler Simonsen
Henrik Køhler Simonsen is Head of Department and Head of Lif Education, Lif Exhibition and Medicademy.
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Lif Education, Diploma in Basic Pharmaceutical Medicine, Clinical Research, Drug Development, Medicademy Pharmacovigilance, Medicademy Regulatory Affairs, RA, PV, Pharmacovigilance, Regulatory Affairs
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