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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 Contact
COURSE CALENDAR NEWS
1 January 2012:
Regulatory Affairs Network Group
Only a limited number of seats available! Application still possible!
» Read more
29 May 2012:
Medicademy Module R9: Product Life Cycle Activities
» Read more
1 June 2012:
Exam: Medicademy Module R8: Clinical Development and Documentation
» Read more
6 June 2012:
Exam: Module 5. Preclinical and Clinical Aspects of Pharmacovigilance
» Read more
12 June 2012:
Exam: Medicademy Module R1: The Pharmaceutical Law Frames in the EU
» Read more
28 August 2012:
Medicademy Pharmacovigilance Module 6: Pharmacovigilance data in Application and Registration
» Read more
3 September 2012:
Exam: Medicademy Module R9: Product Life Cycle Activities
» Read more
5 September 2012:
Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
» Read more
21 September 2012:
Hot Topic Seminar - Latest News within the Pharmacovigilance Legislation
» Read more
25 September 2012:
Exam: Module 6. Pharmacovigilance Data in Application and Registration
» Read more
27 September 2012:
Medicademy Module R11: Roles and Responsibilities of a Regulatory Affairs Professional
» Read more
8 October 2012:
Exam: Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
» Read more
9 October 2012:
Medicademy Module R12: Medical Devices - Drug/Device Combinations
» Read more
29 October 2012:
Exam: Medicademy Module R11: Role and Responsibilities of a Regulatory Affairs Professional
» Read more
5 November 2012:
Exam: Medicademy Module R12: Medical Devices - Drug/Device Combinations
» Read more
7 November 2012:
Medicademy Module R15: The Regulatory Affairs Environment for Generic Products in the EU
» Read more
13 November 2012:
Medicademy Pharmacovigilance Module 4: Post-Marketing Surveillance
» Read more
27 November 2012:
Medicademy Pharmacovigilance Modul 8: Veterinary Pharmacovigilance
» Read more
3 December 2012:
Medicademy Module R6: Quality - Drug Substance and Drug Product
» Read more
12 December 2012:
Exam: Module 4. Post-Marketing Surveillance
» Read more
7 January 2013:
Exam: Medicademy Module R6: Quality - Drug Substance and Drug Product
» Read more
5 February 2013:
Medicademy Pharmacovigilance Module 7. Adverse Drug Reactions by Body Systems
» Read more
6 February 2013:
Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
» Read more
27 February 2013:
Medicademy Module R14: Veterinary Regulatory Affairs in the EU
» Read more
12 March 2013:
Exam: Medicademy Module R10: Biopharmaceuticals - Quality Development and Documentation
» Read more
19 March 2013:
Medicademy Pharmacovigilance Module 1. Principles of Pharmacovigilance
» Read more
5 April 2013:
Exam: Medicademy Module R14: Veterinary Regulatory Affairs in the EU
» Read more
10 April 2013:
Medicademy Module R3: The Regulatory Affairs Environment in the USA
» Read more
13 May 2013:
Exam: Medicademy Module R3: The Regulatory Affairs Environment in the USA
» Read more
14 May 2013:
Medicademy Pharmacovigilance Module 3: Pharmacoep­idemiology
» Read more
COURSE CALENDAR NEWS
20 April 2012:
Latest News within the Pharmacoviglance Legislation
New Pharmacovigilance Legislation!... » Read more
Read all news here
 
Uddannelsesmuligheder
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
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
Contact
Lersø Parkallé 101    DK-2100 Copenhagen    Phone: +45 39 15 09 10    Fax: +45 39 27 60 70    mail@medicademy.net