In the post-xEVMPD regulatory context, Wim Cypers, VP Regulatory Affairs at ArisGlobal, outlines what the future holds in terms of regulatory submission tracking and management. Mere compliance with a regulatory deadline is not going to be enough. Progressive regulatory affairs teams look to strategically contribute to the success of their organisations. Compliance with XEVMPD regulation and preparation for the more comprehensive and global ISO-IDMP standards is just such a once-in-a-generation opportunity. Wim then explains ArisGlobal’s perspective on how to strategize and optimize the resources deployed for XEVMPD to move on… and up.