Aim
The course provides a comprehensive overview of the requirements and critical issues regarding non-clinical studies that supports clinical 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 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/Non-clinical-development-and-d/3874/0/
Categories
Enabling Technologies: Preclinical studies
Methodology: Laboratory animal techniques
Target Group
All researchers
Country
DK
City
Copenhagen
More information
view website