Product Life Cycle Activities 

Aim

The course provides comprehensive knowledge of the basis for evaluating the possibilities and consequences of different types of Life Cycle activities and subsequently to plan and perform the activities related to the regulatory maintenance of the product.

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 5.00
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/Product-life-cycle-activities/3870/0/