FDA & CFIA 2016 Regulatory Changes/Updates 2017

  • 17 Mar 2017
  • Webinar

Description

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

Past Events

Important

Please, check "FDA & CFIA 2016 Regulatory Changes/Updates" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Pharma
Industry: Food & Beverages

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