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Exam: Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
27 February 2012:
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Medicademy Module R7: Non-clinical Development and Documentation
29 February 2012:
EXTENDED DEADLINE FOR APPLICATION - FEBRUARY 24, 2012!
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Exam: Medicademy Module R7: Non-clinical Development and Documentation
13 April 2012:
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Hot Topic Seminar on Falsified Medicines
20 April 2012:
- How can we prevent it?
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Medicademy Module R8: Clinical Development and Documentation
24 April 2012:
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Medicademy Pharmacovigilance Module 5: Preclinical and Clinical Aspects of Pharmacovigilance
8 May 2012:
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Medicademy Module R1: The Pharmaceutical Law Frames in the EU
9 May 2012:
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Exam: Medicademy Module R8: Clinical Development and Documentation
28 May 2012:
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Medicademy Module R9: Product Life Cycle Activities
29 May 2012:
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Exam: Module 5. Preclinical and Clinical Aspects of Pharmacovigilance
7 June 2012:
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Exam: Medicademy Module R1: The Pharmaceutical Law Frames in the EU
12 June 2012:
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Medicademy Pharmacovigilance Module 6: Pharmacovigilance data in Application and Registration
28 August 2012:
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Exam: Medicademy Module R9: Product Life Cycle Activities
3 September 2012:
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Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
5 September 2012:
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Exam: Module 6. Pharmacovigilance Data in Application and Registration
25 September 2012:
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Medicademy Module R11: Roles and Responsibilities of a Regulatory Affairs Professional
27 September 2012:
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Exam: Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
8 October 2012:
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Medicademy Module R12: Medical Devices - Drug/Device Combinations
9 October 2012:
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Exam: Medicademy Module R12: Medical Devices - Drug/Device Combinations
5 November 2012:
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Medicademy Pharmacovigilance Module 4: Post-Marketing Surveillance
13 November 2012:
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Medicademy Module R6: Quality - Drug Substance and Drug Product
3 December 2012:
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Exam: Module 4. Post-Marketing Surveillance
12 December 2012:
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Exam: Medicademy Module R6: Quality - Drug Substance and Drug Product
7 January 2013:
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Medicademy Pharmacovigilance Module 7. Adverse Drug Reactions by Body Systems
5 February 2013:
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Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
6 February 2013:
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Medicademy Module R14: Veterinary Regulatory Affairs in the EU
27 February 2013:
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Medicademy Pharmacovigilance Module 1. Principles of Pharmacovigilance
5 March 2013:
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Exam: Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
12 March 2013:
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Exam: Medicademy Module R14: Veterinary Regulatory Affairs in the EU
5 April 2013:
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Medicademy Module R3: The Regulatory Affairs Environment in the USA
10 April 2013:
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Exam: Medicademy Module R3: The Regulatory Affairs Environment in the USA
13 May 2013:
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Medicademy Pharmacovigilance Module 2: Pharmacovigilance Systems - A Hands-On Approach
14 May 2013:
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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)?
5 June 2013:
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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)?
2 September 2013:
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Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
3 October 2013:
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Exam: Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
4 November 2013:
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Regulatory Affairs
Pharmacovigilance
Individual Courses
SEE THE COURSE CALENDAR HERE
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
TAGS
Lif Education, Diploma in Basic Pharmaceutical Medicine, Clinical Research, Drug Development, Medicademy Pharmacovigilance, Medicademy Regulatory Affairs, RA, PV, Pharmacovigilance, Regulatory Affairs
Regulatory Affairs
Course overview
About R.A.
Requirements
MPRA
Diploma
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News
Pharmacovigilance
About Pharmacovigilance
Course Overview
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Diploma
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About
About Medicademy
About Lif
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Contact
Lersø Parkallé 101 DK-2100 Copenhagen Phone: +45 39 15 09 10 Fax. +45 39 27 60 70
mail@medicademy.net