How do drugs and medical devices go from lab to clinical use? What research is required to get them to patients and demonstrate safety and effectiveness along the way? This course allows students to gain knowledge and understanding of the drug development process, the regulatory framework and explore the differences between drugs and medical devices.
- Legislation on the drug approval process
- Phases of drug and medical device development
- The pre-clinical and clinical activities required for drug approval
- Clinical trial outputs - safety and efficacy data and interpretation
Individual Course Registration
This course is part of the Diploma program and can also be taken as an individual course for non-credit/professional development. How many courses can you take before you have to apply to the program?