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Course overview About R.A. Requirements MPRA Diploma Individual Modules Steering Committee Faculty
About Pharmacovigilance Course Overview Entry Requirements Diploma Individual Modules Steering Committee Faculty
About Medicademy About Lif Course Structure Examination Course Facilities, Accomodation, Transportation and Networkding Dinner Contact
CALENDAR NEWS SEMINARS
1 January 2013:
Pharmacovigilance Networking Group
» Read more
1 January 2013:
Regulatory Affairs Network Group 2013
Only a limited number of seats!
» Read more
29 May 2013:
Medicademy Module R13: The Regulatory Environment in Major Markets Outside the ICH - How to optimize your Regulatory Strategy dealing with the BRIC Countries (Brazil, Russia, India and China)
» Read more
11 June 2013:
Exam: Module 3. Pharmacoep­idemiology
» Read more
21 June 2013:
Exam: Medicademy Module R1: The Pharmaceutical Law Frames in the EU
» Read more
2 September 2013:
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)
» Read more
4 September 2013:
Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
» Read more
12 September 2013:
Hot Topic Seminar on EU Pharmacovigilance Legislation - Have we achieved what we expected
» Read more
17 September 2013:
Medicademy Pharmacovigilance Module 6: Pharmacovigilance data in Application and Registration
» Read more
1 October 2013:
FreeLearn Regulatory Affairs
- gratis læring hvor som helst, når som helst
» Read more
3 October 2013:
Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
» Read more
8 October 2013:
Medicademy Pharmacovigilance Module 2: Pharmacovigilance Systems - A Hands-On Approach
» Read more
11 October 2013:
Exam: Module 6. Pharmacovigilance Data in Application and Registration
» Read more
22 October 2013:
Medicademy Pharmacovigilance Module 7. Adverse Drug Reactions by Body Systems
» Read more
23 October 2013:
Medicademy Module R14: Veterinary Regulatory Affairs in the EU
» Read more
4 November 2013:
Exam: Medicademy Module R5: Regulatory Strategic Considerations during Global Drug Development
» Read more
7 November 2013:
Exam: Module 2. Pharmacovigilance Systems - A Hands-On Approach
» Read more
11 November 2013:
Medicademy Module R7: Non-clinical Development and Documentation
» Read more
20 November 2013:
Exam: Module 7. Adverse Drug Reactions by Body Systems
» Read more
25 November 2013:
Exam: Medicademy Module R14: Veterinary Regulatory Affairs in the EU
» Read more
2 December 2013:
Medicademy Module R8: Clinical Development and Documentation
» Read more
13 December 2013:
Exam: Medicademy Module R7: Non-clinical Development and Documentation
» Read more
6 January 2014:
Exam: Medicademy Module R8: Clinical Development and Documentation
» Read more
22 January 2014:
Medicademy Module R9: Product Life Cycle Activities
» Read more
24 February 2014:
Exam: Medicademy Module R9: Product Life Cycle Activities
» Read more
25 February 2014:
Medicademy Pharmacovigilance Module 5: Preclinical and Clinical Aspects of Pharmacovigilance
» Read more
27 March 2014:
Exam: Module 5. Preclinical and Clinical Aspects of Pharmacovigilance
» Read more
8 April 2014:
Medicademy Pharmacovigilance Modul 8: Veterinary Pharmacovigilance
(Preliminary date)
» Read more
20 May 2014:
Medicademy Pharmacovigilance Module 1. Principles of Pharmacovigilance
» Read more
23 September 2014:
Medicademy Pharmacovigilance Module 4, Post-Marketing Surveillance
(Preliminary date)
» Read more
CALENDAR NEWS SEMINARS
20 April 2012:
Latest News within the Pharmacoviglance Legislation
New Pharmacovigilance Legislation!... » Read more
Read all news here
CALENDAR NEWS SEMINARS
17 October 2012:
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Uddannelsesmuligheder
Regulatory Affairs
Pharmacovigilance
Individual Courses
E-learning
SEE THE COURSE CALENDAR HERE

TESTIMONIALS

Stine Folkenberg Hedegaard

Stine Folkenberg Hedegaard is E-learning Manager and responsible for e-learning, communication, marketing and a number of courses.
 
sfh@dli.dk
Phone: +45 39 15 09 27

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
Page Content
Regulatory Affairs
Course overview
About R.A.
Requirements
MPRA
Diploma
Individual Modules
Steering Committee
Faculty
Pharmacovigilance
About Pharmacovigilance
Course Overview
Entry Requirements
Diploma
Individual Modules
Steering Committee
Faculty
About
About Medicademy
About Lif
Course Structure
Examination
Course Facilities, Accomodation, Transportation and Networkding Dinner
Contact
Lersø Parkallé 101    DK-2100 Copenhagen    Phone: +45 39 15 09 10    Fax: +45 39 27 60 70    mail@medicademy.net