Medical Devices (WS17)

2 May 2018
Available Seats:

The attendee will be able to:

  1. List no fewer than two (2) Code of Federal Regulations (CFR) that cover devices for approval.
  2. Explain what regulators are looking for to show device GMPs are in a state of control.
  3. Describe how devices can be blinded in order to ensure positive statistical significance at the end of the trial.

Become a member

Global Clinical Supplies Group

Join GCSG for full access...

to our educational resources, conference materials and our directory of more than 480 Clinical Supply colleagues. Experience the culture of collaboration, It only takes approximately 3 minutes 22 seconds.

Please note that membership is included and FREE of charge when you sign up for an event.