• Getting Ready for IDMP Compliance

    The impact of regulatory compliance on development of pharmaceutical and life sciences products is getting convergent and complex. It takes thorough analysis and ample amount of time and resources to understand a particular guidance and its implementation to be able to get compliant as per health authorities guidelines. With an aim to bring significant improvements, the year of 2012 witnessed approval of ISO IDMP that was intended to substitute the XEVMPD in Europe and the Electronic Drug Registration and Listing System (eDRLS) in the United States.