Regulatory Information Management 2013

Regulatory Information Management 2013 is a conference addresses topics to ensure that your regulatory processes are efficient and compliant including:

• Communication and information flow between affiliate and headquarter
• Regulatory Information Management 2013 in practice
• EVMPD compliance and preparation for IDMP
• Managing RIM systems during mergers, acquisitions and in/out licensing
• Planning and tracking efficiencies
• Regulatory Information Management 2013 data entry models
• Validation and archiving

Who should Attend

Directors, Heads of Department, Team Leaders, Managers, Consultants, Associates and Coordinators from: Global Drug Regulatory Affairs, Regulatory Affairs, Worldwide Regulatory Affairs, International Regulatory Affairs, Regulatory Information/Data Management, Regulatory Operations, Systems Engineering, Regulatory Information Systems, International Strategy, Registration and Business Development.