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Exam: Medicademy Module R2: EU Applications for Marketing Authorisations, Paediatric Investigation Plans, Clinical Trials and Orphan Drug Designation
Registration deadline:
4 October 2012
Register:
Registration is closed
Startdate:
8 October 2012
Mail us for more information
Plads til diskussion – rigtig godt
Ann-Lisbeth Aarup Nielsen - ALK-Albelló - Regulatory Affairs Officer
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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
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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
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