Role and Responsibilities of a Regulatory Affairs-professional

Aim

The course provides comprehensive knowledge regarding role and responsibilities of regulatory affairs professionals in all aspects of a drug development process and product life cycle management.

Location & Organization

Organizer

MPRA – Master of Pharmaceutical Regulatory Affairs

Location / venue

University of Copenhagen (Faculty of Health and Medical Sciences)

Timing & Workload

Duration Segmental
ECTS points 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

The applicant must have a relevant educational background at Bachelor level and at least 2 years experience within Drug Regulatory Affairs or equivalent qualifications

More Information

http://www.farma.ku.dk/index.php/Role-and-responsibilities-of-a/3876/0/