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Diploma in Pharmacovigilance
A Diploma in Pharmacovigilance will provide you with a profound knowledge of drug safety. You will learn how to find, assess, understand and prevent adverse effects and harmful side effects, and you will be able to review information from pharmaceutical companies.
The diploma programme will give you an overview of the pre-clinical and clinical aspects of pharmacovigilance, and principles, systems, and post-marketing surveillance will be thoroughly reviewed.
The diploma consists of 5 modules of own choice, choose between:
- Module 1: Principles of Pharmacovigilance
- Module 2: Pharmacovigilance Systems - A Hands-On Approach
- Module 3: Pharmacoepidemiology
- Module 4: Post-Marketing Surveillance
- Module 5: Pre-Clinical and Clinical Aspects of Pharmacovigilance
- Module 6: Pharmacovigilance Data in Application and Registration
- Module 7: Adverse Drug Reactions by Body Systems
- Module 8: Veterinary Pharmacovigilance
The diploma programme is aimed at pharmacovigilance employees with several years of experience and employees with a relevant Bachelor Degree. Employees with similar qualifications, who wish to further develop their competencies within drug safety, will also benefit from this programme.
To obtain a Diploma in Pharmacovigilance, students must pass five modules of own choice, including the examinations, within 5 years. One module from the Medicademy Regulatory Affairs programme may be included in the Medicademy Pharmacovigilance Diploma.
Public Affairs Seminar
1 June 2012:
Sådan påvirkes og samarbejdes med forskellige interessenter af relevans for lægemiddelindustrien
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Medicademy Pharmacovigilance Module 6: Pharmacovigilance data in Application and Registration
28 August 2012:
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Introduktion til lægemiddelregistrering
13 September 2012:
Vil du gerne vide mere om lægemiddelregistrering og -lovgivning i EU? Dette kursus hjælper dig til at forstå registreringsansøgninger og procedurer, vedligeholdelse af godkendte lægemidler og en registreringsafdelings mange opgaver.
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Kritisk artikellæsning, September 2012
13 September 2012:
Læser du ofte videnskabelige artikler? Og har du brug for at kunne gennemskue kvaliteten og fortolke resultaterne af de læste artikler? Så er dette kursus lige noget for dig.
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Hot Topic Seminar - Latest News within the Pharmacovigilance Legislation
21 September 2012:
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Medicademy Pharmacovigilance Module 4: Post-Marketing Surveillance
13 November 2012:
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Personal Workflow
13 November 2012:
Are you pinned down by long and stressful workdays? Have you lost track of all your commitments? Do you want to accomplish more and work less? Then this course is what you need to regain focus and energy.
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Medicademy Pharmacovigilance Modul 8: Veterinary Pharmacovigilance
27 November 2012:
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Critical Review of Articles, December 2012
6 December 2012:
Do you often have to read and understand scientific articles? Do you find it difficult to evaluate their quality and interpret their results? Then this is the course for you.
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Medicademy Pharmacovigilance Module 7. Adverse Drug Reactions by Body Systems
5 February 2013:
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Medicademy Pharmacovigilance Module 1. Principles of Pharmacovigilance
19 March 2013:
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Medicademy Pharmacovigilance Module 3: Pharmacoepidemiology
14 May 2013:
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Medicademy Pharmacovigilance Module 2: Pharmacovigilance Systems - A Hands-On Approach
8 October 2013:
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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
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