Hugh Collins, Senior Account Executive & Navee Sarabu, Director, Product Management & Strategy, Liaison Healthcare
Most life sciences companies are challenged with meeting European Medicines Agency’s Identification of Medicinal Products (IDMP) regulatory requirement in 2016, especially since the standard hasn’t been finalized!
While many are taking a wait and see approach, others are getting a jump start in figuring out the 5Ws about the data necessary to comply and beginning to execute a plan for success. This means both domain expertise and technology.
Attend our upcoming webinar to learn:
the Who, What, When, Where and Why about IDMP
how to get started given the standard has not been finalized
how utilizing cloud-based solutions speed up data integration and aggregation, and
how IDMP provides the on-ramp to address broader data management and regulatory compliance strategies.
There is very little time for those governed by the mandate to design and implement the enterprise-wide data management processes needed to aggregate, cleanse, validate and ultimately syndicate product data..