Medical Devices (WS17)
- Date:
- 1 May 2018
- Time:
- -
- Available Seats:
- 29
The attendee will be able to:
- List no fewer than two (2) Code of Federal Regulations (CFR) that cover devices for approval.
- Explain what regulators are looking for to show device GMPs are in a state of control.
- Describe how devices can be blinded in order to ensure positive statistical significance at the end of the trial.
