Published September 2015

Our Expert Franck Toussaint to be speaker at the 2015 "Bio Supply Management Alliance" next Ocotber in San Francisco

“ID for Medicinal Products: Preparing for the EMA Regulation”:  EMA standard called IDMP created by ISO which takes 2017-18.  One of the purposes of this regulation is to establish standards (“controlled vocabularies”) across the industry for batch and lot identifiers, covering 243 attributes and 7 categories (e.g. drug substance, drug product, etc.).  This regulation will impact many functional groups within pharmaceutical companies (including Supply Chain), and applies to both clinical and commercial products.