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Collapse Medicademy PharmacovigilanceMedicademy Pharmacovigilance
Collapse Diploma in PharmacovigilanceDiploma in Pharmacovigilance
Hot Topic Seminar on Falsified Medicines
Medicademy Pharmacovigilance Module 5: Preclinical and Clinical Aspects of Pharmacovigilance
Public Affairs Seminar
Medicademy Pharmacovigilance Module 6: Pharmacovigilance data in Application and Registration
Kritisk artikellæsning, September 2012
Medicademy Pharmacovigilance Module 4: Post-Marketing Surveillance
Medicademy Pharmacovigilance Module 7. Adverse Drug Reactions by Body Systems
Medicademy Pharmacovigilance Module 1. Principles of Pharmacovigilance
Medicademy Pharmacovigilance Module 2: Pharmacovigilance Systems - A Hands-On Approach
Collapse Medicademy Regulatory AffairsMedicademy Regulatory Affairs
Collapse Diploma in Regulatory AffairsDiploma in Regulatory Affairs
Regulatory Affairs Network Group
Exam: Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
Medicademy Module R7: Non-clinical Development and Documentation
Exam: Medicademy Module R7: Non-clinical Development and Documentation
Hot Topic Seminar on Falsified Medicines
Medicademy Module R8: Clinical Development and Documentation
Medicademy Module R1: The Pharmaceutical Law Frames in the EU
Exam: Medicademy Module R8: Clinical Development and Documentation
Medicademy Module R9: Product Life Cycle Activities
Public Affairs Seminar
Exam: Medicademy Module R1: The Pharmaceutical Law Frames in the EU
Exam: Medicademy Module R9: Product Life Cycle Activities
Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
Kritisk artikellæsning, September 2012
Medicademy Module R11: Roles and Responsibilities of a Regulatory Affairs Professional
Exam: Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
Medicademy Module R12: Medical Devices - Drug/Device Combinations
Exam: Medicademy Module R12: Medical Devices - Drug/Device Combinations
Medicademy Module R6: Quality - Drug Substance and Drug Product
Exam: Medicademy Module R6: Quality - Drug Substance and Drug Product
Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
Medicademy Module R14: Veterinary Regulatory Affairs in the EU
Exam: Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
Exam: Medicademy Module R14: Veterinary Regulatory Affairs in the EU
Medicademy Module R3: The Regulatory Affairs Environment in the USA
Exam: Medicademy Module R3: The Regulatory Affairs Environment in the USA
Medicademy Module R13: The Regulatory Environment in Major Markets outside ICH - How you can optimise your regulatory strategy dealing with the BRIC Countries (Brazil, Russia, India and China)?
Exam: Medicademy Module R13: The Regulatory Environment in Major Markets outside ICH - How you can optimise your regulatory strategy dealing with the BRIC Countries (Brazil, Russia, India and China)?
Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
Exam: Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
Medicademy Module R4: The Regulatory Affairs Environment in Japan
Exam: Medicademy Module R4: The Regulatory Affairs Environment in Japan
Collapse Individual Modules Regulatory AffairsIndividual Modules Regulatory Affairs
Medicademy Module R7: Non-clinical Development and Documentation
Hot Topic Seminar on Falsified Medicines
Medicademy Module R8: Clinical Development and Documentation
Medicademy Module R1: The Pharmaceutical Law Frames in the EU
Public Affairs Seminar
Exam: Medicademy Module R1: The Pharmaceutical Law Frames in the EU
Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
Exam: Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
Medicademy Module R12: Medical Devices - Drug/Device Combinations
Exam: Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
Medicademy Module R3: The Regulatory Affairs Environment in the USA
Exam: Medicademy Module R13: The Regulatory Environment in Major Markets outside ICH - How you can optimise your regulatory strategy dealing with the BRIC Countries (Brazil, Russia, India and China)?
Collapse Master of Pharmaceutical Regulatory AffairsMaster of Pharmaceutical Regulatory Affairs
Regulatory Affairs Network Group
Exam: Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
Medicademy Module R7: Non-clinical Development and Documentation
Exam: Medicademy Module R7: Non-clinical Development and Documentation
Hot Topic Seminar on Falsified Medicines
Medicademy Module R8: Clinical Development and Documentation
Medicademy Module R1: The Pharmaceutical Law Frames in the EU
Exam: Medicademy Module R8: Clinical Development and Documentation
Medicademy Module R9: Product Life Cycle Activities
Exam: Medicademy Module R1: The Pharmaceutical Law Frames in the EU
Exam: Medicademy Module R9: Product Life Cycle Activities
Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
Medicademy Module R11: Roles and Responsibilities of a Regulatory Affairs Professional
Exam: Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
Medicademy Module R12: Medical Devices - Drug/Device Combinations
Exam: Medicademy Module R12: Medical Devices - Drug/Device Combinations
Medicademy Module R6: Quality - Drug Substance and Drug Product
Exam: Medicademy Module R6: Quality - Drug Substance and Drug Product
Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
Medicademy Module R14: Veterinary Regulatory Affairs in the EU
Exam: Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
Exam: Medicademy Module R14: Veterinary Regulatory Affairs in the EU
Medicademy Module R3: The Regulatory Affairs Environment in the USA
Exam: Medicademy Module R3: The Regulatory Affairs Environment in the USA
Medicademy Module R13: The Regulatory Environment in Major Markets outside ICH - How you can optimise your regulatory strategy dealing with the BRIC Countries (Brazil, Russia, India and China)?
Exam: Medicademy Module R13: The Regulatory Environment in Major Markets outside ICH - How you can optimise your regulatory strategy dealing with the BRIC Countries (Brazil, Russia, India and China)?
Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
Exam: Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
Medicademy Module R4: The Regulatory Affairs Environment in Japan
Exam: Medicademy Module R4: The Regulatory Affairs Environment in Japan

Helle Rishøj Nielsen

Helle Rishøj Nielsen is Payroll Officer and is responsible for payroll, travel arrangements, evaluations, diplomas and certificates, etc.
 
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.
 
Phone: +45 39 15 09 28

Tina Jensen

Tina Jensen is Program Director, Medicademy Regulatory Affairs and responsible for Introduction to Drug Registration.
 
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.
 
Phone: +45 39 15 09 45
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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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Lersø Parkallé 101    DK-2100 Copenhagen    Phone: +45 39 15 09 10    Fax. +45 39 27 60 70    mail@medicademy.net