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What is Hot in Global Labeling?


This webinar will provide highlights of draft and recently approved regulations for awareness of potential impact to your global operations. This includes the revisions to the EU GVP Module IX guideline, SPL in Canada, updating of labeling in Japan and device regulations in the EU.

Continuing Education Credits are not available for this event.

Featured topics

• Labeling Regulation and Guidance Changes Globally

Who should attend?

Professionals from biopharmaceutical and device companies, regulatory authorities, CROs, and consulting agencies involved in:

  • Labeling
  • Clinical Safety/pharmacovigilance
  • Pharmacoepidemiology
  • Regulatory affairs/drug review and approval process
  • Medical affairs and communications
  • Medical writing
  • Clinical research and development
  • Product research and development alliances
  • Quality control/quality asssurance

Learning objectives

At the conclusion of this webinar, participants should be able to:
  • Identify new or recently revised regulations impacting labeling
  • Identify potential impact of regulation/guidance changes on participants’ labeling operations
  • Understand how these issues shaped the agenda for the DIA Global Labeling Conference in April 2018

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