The Regulatory Affairs Certificate: Medical Devices and Pharmaceuticals, provides route for you to achieve both tracks in an efficient manner. By taking all six core courses and selecting eight electives, you have the opportunity to extend your achievement with a dual certificate acquired in a 12-month timeframe.
The Regulatory Affairs Certificate: Medical Devices and Pharmaceuticals is achieved by completing six (6) core and eight (8) elective courses. After successfully completing all 14 courses, you will receive a certificate recognizing your achievement.
You will have 12 months
to complete all 14 courses.
The following six courses are required as part of the program requirements:
- Global Regulatory Strategy for Medical Devices
- Global Regulatory Strategy for Pharmaceuticals
- Medical Devices: Definition & Lifecycle
- Pharmaceuticals: Definition & Lifecycle
- Role of the Regulatory Professional
You also choose eight courses from our entire portfolio of programs
. These courses can be labeled with a M, P or M/P. This means that these courses are valid electives in order to achieve the dual certificate.
Upgrade to a Dual Certificate
Upgrade Online (Medical Devices)
Upgrade Online (Pharmaceuticals)