FDA & CFIA 2016 Regulatory Changes/Updates 2017 is a webinar that covers topics such as:
- 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
FDA & CFIA 2016 Regulatory Changes/Updates 2017 is intended for:
- 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