Webcast Replay: 2012

Moving on... and up!: The present and future of electronic submissions in ISO-IDMP paradigm

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...Read More »

XEVMPD - Q&A with Andrew Marr

Continuing the series of webcasts on the XEVMPD regulation, industry expert Andrew Marr, PhD joined Wim Cypers, VP Regulatory Affairs, for a one-hour, free-wheeling question and answer session with Regulatory Affairs professionals from many large, medium and small pharmaceutical companies. Andrew began the session with a brief overview of the...Read More »