Program Requirements
General Program Requirements:
Number of Credits Required Beyond the Baccalaureate:Ìý30
Required Courses:
Code | Title | Credit Hours |
---|---|---|
Core Courses | ||
²Ï´¡¸é´¡Ìý5459 | Drug Development | 3 |
²Ï´¡¸é´¡Ìý5508 | Good Pharmacovigilance Operations | 3 |
²Ï´¡¸é´¡Ìý5536 | Good Clinical Practices | 3 |
²Ï´¡¸é´¡Ìý5537 | Clinical Trial Management | 3 |
²Ï´¡¸é´¡Ìý5538 | Clinical Drug Safety and Pharmacovigilance | 3 |
´Ç°ùÌý²Ï´¡¸é´¡Ìý5571 | Post-Marketing Safety Surveillance | |
²Ï´¡¸é´¡Ìý5573 | Pharmacoepidemiology | 3 |
²Ï´¡¸é´¡Ìý5578 | Benefit Risk Management and Safety Signaling of Healthcare Products | 3 |
²Ï´¡¸é´¡Ìý5579 | Regulatory and Legal Basis of Pharmacovigilance | 3 |
Electives | ||
Select from the following approved courses: | 6 | |
±Ê±ÊÌý±Ê312 | ADRS Organ Systems Appr | |
±Ê±ÊÌý±Ê313 | Clin Pharmacokinetics | |
²Ï´¡¸é´¡Ìý5497 | Statistics for Clinical Trials 1 | |
²Ï´¡¸é´¡Ìý5539 | Global Clinical Drug Development | |
²Ï´¡¸é´¡Ìý5547 | Project Management for Clinical Trials | |
²Ï´¡¸é´¡Ìý5612 | Bioethics for Pharmaceutical Professionals | |
²Ï´¡¸é´¡Ìý5618 | Clinical Data Management (CDM) | |
Total Credit Hours | 30 |
- 1
Alternately, students may take ±Ê±ÊÌý±Ê254 Bio Stat/Med Lit Eval.
Culminating Event: Successful completion of coursework is required to earn the MS in Global Clinical and Pharmacovigilance Regulations.