Course: Safety of Medicines - From Non-Clinical Development to Pharmacovigilance – University of Copenhagen

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Course: Safety of Medicines - From Non-Clinical Development to Pharmacovigilance

The content of this course covers the regulatory issues concerning non-clinical development up to post marketing pharmacovigilance, with emphasis on regulatory issues concerning clinical development and pharmacovigilance.

After completion the student will be able to account for, scientifically discuss, advise on and evaluate the role of non-clinical safety, clinical and epidemiological scientific safety assessments as the basis for the continuing safety assessment of medicines.

The course is a part of the Master of Medicines Regulatory Affairs, but it can also be chosen as a single course.

For more information regarding the course content, registration and other practical details, visit the course’s page.