Clinical Material Challenges for Devices and Drug/Device Combinations

Date:
29 April 2015
Time:
-
Available Seats:
30

Learning Objectives

● Compare and contrast the challenges presented by packaging devices or drug/device combinations versus traditional IMP.
● Differentiate the regulatory requirements for devices or drug/device combinations versus traditional IMP.
● Give examples of at least two (2) challenges involved in the import/export of devices or drug/device combinations compared to traditional IMP.

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