June 30 - July 1, 2014    Munich , Germany
Create a sustainable strategy for linking regulatory systems and establishing an efficient interface between various departments by aligning data and responsibilities between departments
Discuss best ways for running pre-projects seeing whether eVMPD capable systems would be able to handle the ISO IDMP requirements

Inform yourself as to new IT and data management software tools and concepts – such as Cloud and software services – to improve your process and comply with regulations!

Explore considerations for identifying and authorizing products for different countries by improving master data management process in your company

Learn how Process Excellence methods such as LEAN Six Sigma can support integration of new information processes and enhance the efficiency of information management across multiple business units

Speakers: Managing Director, Merck, Director, Timm Pauli, Regulatory Informatics and Submission Management, Jörg Schnitzler, Head of Regulatory Affairs Operations, Boehringer Ingelheim Pharma, Andrew Marr, Marr Consultancy

Price: €2.449

Time: 09:00-17:00

Venue

Location: Pullman Munich
Contact Theodor-Dombart-Straße 4, 80805 München, Germany Munich , Germany
+49 89 360990

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Regulatory Process Excellence Pharma June 30 - July 1, 2014