Understanding Your Responsibilities as Importer of Record (IOR) (WS03)

Date:
21 September 2020
Time:
-
Available Seats:
35

Importation and movement of clinical supplies internationally will typically bring up questions about ownership of supplies, importation processes and Importer of Record (IOR) responsibilities. Knowing the specific obligations of the sponsor, clinical research organizations (CRO) and vendors will help to ensure maximum efficiencies when importing. This workshop will clarify the responsibilities surrounding IOR and ownership of clinical trial materials.

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.