The ISO published Identification of Medicinal Products (IDMP) standards almost a year ago (November 2012). EMA’s Extended EudraVigilance Medicinal Product Dictionary (XEVMPD) have also been in currency for almost 1.5 years i.e. since July 02, 2012. However, the compliance efforts for XEVMPD and readiness for IDMP still leaves lot to be desired.
In this webcast, industry thought leader Dr. Andrew Marr and Mr. Wim Cypers, Vice President, Regulatory Affairs, ArisGlobal discussed how and why will 2014 be a year of significant effort by all concerned to get the data into usable condition and to maintain them for XEVMPD compliance and in preparation of IDMP compliance. They outlined how regulatory authorities, industry and software vendors can work collaboratively to achieve these goals.