FDA & CFIA 2016 Regulatory Changes/Updates 2017

Topics

• Learn the latest terminology and acronyms
• The latest regulatory changes and requirements
• Determine current risk level and how to remain compliant
• How does this affect global trade facilitation?
• Determine if your medical devices are marked and registered compliantly
• Learn the latest product marking requirements
• Changes from June, July, August, and upcoming important dates

Who should Attend

• Validation specialists
• Internal regulatory departments
• Quality control professionals
• Documentation specialists
• FDA professionals
• Medical devices professionals
• Global tax professionals
• Finance professionals
• Logistics managers
• Trade compliance professionals
• Import/export professionals
• Company compliance officers
• Brokers and forwarders
• Global trade professionals
• Companies engaged in global trade
• Professionals who are looking for risk reduction, time and cost savings