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1 January 2012:
Regulatory Affairs Network Group
Only a limited number of seats available! Application still possible!
» Read more
27 February 2012:
Exam: Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
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29 February 2012:
Medicademy Module R7: Non-clinical Development and Documentation
EXTENDED DEADLINE FOR APPLICATION - FEBRUARY 24, 2012!
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13 April 2012:
Exam: Medicademy Module R7: Non-clinical Development and Documentation
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20 April 2012:
Hot Topic Seminar on Falsified Medicines
- How can we prevent it?
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24 April 2012:
Medicademy Module R8: Clinical Development and Documentation
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8 May 2012:
Medicademy Pharmacovigilance Module 5: Preclinical and Clinical Aspects of Pharmacovigilance
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9 May 2012:
Medicademy Module R1: The Pharmaceutical Law Frames in the EU
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28 May 2012:
Exam: Medicademy Module R8: Clinical Development and Documentation
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29 May 2012:
Medicademy Module R9: Product Life Cycle Activities
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7 June 2012:
Exam: Module 5. Preclinical and Clinical Aspects of Pharmacovigilance
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12 June 2012:
Exam: Medicademy Module R1: The Pharmaceutical Law Frames in the EU
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28 August 2012:
Medicademy Pharmacovigilance Module 6: Pharmacovigilance data in Application and Registration
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3 September 2012:
Exam: Medicademy Module R9: Product Life Cycle Activities
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5 September 2012:
Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
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25 September 2012:
Exam: Module 6. Pharmacovigilance Data in Application and Registration
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27 September 2012:
Medicademy Module R11: Roles and Responsibilities of a Regulatory Affairs Professional
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9 October 2012:
Medicademy Module R12: Medical Devices - Drug/Device Combinations
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5 November 2012:
Exam: Medicademy Module R12: Medical Devices - Drug/Device Combinations
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13 November 2012:
Medicademy Pharmacovigilance Module 4: Post-Marketing Surveillance
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12 December 2012:
Exam: Module 4. Post-Marketing Surveillance
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5 February 2013:
Medicademy Pharmacovigilance Module 7. Adverse Drug Reactions by Body Systems
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6 February 2013:
Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
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27 February 2013:
Medicademy Module R14: Veterinary Regulatory Affairs in the EU
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5 March 2013:
Medicademy Pharmacovigilance Module 1. Principles of Pharmacovigilance
» Read more
12 March 2013:
Exam: Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
» Read more
5 April 2013:
Exam: Medicademy Module R14: Veterinary Regulatory Affairs in the EU
» Read more
14 May 2013:
Medicademy Pharmacovigilance Module 2: Pharmacovigilance Systems - A Hands-On Approach
» Read more
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Helle Rishøj Nielsen
Helle Rishøj Nielsen is Payroll Officer and is responsible for payroll, travel arrangements, evaluations, diplomas and certificates, etc.
hrn@dli.dk
Phone: +45 39 15 09 11
Minna K. Jørgensen
Minna Kjær Jørgensen is Program Director, Medicademy Pharmacovigilance and also responsible for Introduction to Safety & Pharmacovigilance and Medical Advertising Standards.
mkj@dli.dk
Phone: +45 39 15 09 28
Tina Jensen
Tina Jensen is Program Director, Medicademy Regulatory Affairs and responsible for Introduction to Drug Registration.
tj@medicademy.net
Phone: +45 39 15 09 14
Henrik Køhler Simonsen
Henrik Køhler Simonsen is Head of Department and Head of Lif Education, Lif Exhibition and Medicademy.
hks@dli.dk
Phone: +45 39 15 09 45
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Lersø Parkallé 101 DK-2100 Copenhagen Phone: +45 39 15 09 10 Fax: +45 39 27 60 70
mail@medicademy.net