What is Hot in Global Labeling?
Continuing Education Credits are not available for this event.
Who should attend?
Professionals from biopharmaceutical and device companies, regulatory authorities, CROs, and consulting agencies involved in:
- Clinical Safety/pharmacovigilance
- 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
- 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