Quality - Drug Substance and Drug Product

Aim

The course provides comprehensive, academic knowledge and overview of quality requirements to drug substances and drug products in pharmaceutical drug development.

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 4.00
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/Quality-drug-substance-and-d/3869/0/