Hi all –
Is anyone else having issues obtaining the required supply chain movement documentation for materials procured outside of China for use in clinical trials. Materials procured from our common sourcing vendors have sometimes moved multiple times and we cannot get the full supply chain documents without significant effort and resource regardless of it being in the contract / PO terms that the documentation will be provided. Has anyone else figured out a best practice here? Do all sourcing vendors know of this requirement and request the documents when procuring the material on our behalf?