Drug Regulatory Affairs in Drug Development

Aim

The objective of the course is therefore to give the participants an overall understanding of how the regulatory affairs professionals interplay with all the specialists involved.

Location & Organization

Organizer

MIND - Master of Industrial Drug Development

Course Director

Eva Horn Møller, associate professor, Faculty of Health and Medical Sciences, School of Pharmaceutical Sciences, University of Copenhagen

Location / venue

University of Copenhagen (Faculty of Helth and Medical Sciences)

Timing & Workload

Duration 5 days
ECTS points 2.5
Frequency Annual /biennial
 

Examination yes

Criteria

Is the course taught in English? yes
Is documentation available? (book, syllabus)? yes
Is the course open for external researchers? yes

Remarks

MIND compulsary course

More Information

http://www.farma.ku.dk/index.php/A-8108-Drug-Regulatory-Affairs/1153/0/