BEGIN:VCALENDAR VERSION:2.0 PRODID:-//ChamberMaster//Event Calendar 2.0//EN METHOD:PUBLISH X-PUBLISHED-TTL:P3D REFRESH-INTERVAL:P3D CALSCALE:GREGORIAN BEGIN:VEVENT DTSTART:20160316T130000Z DTEND:20160316T154500Z X-MICROSOFT-CDO-ALLDAYEVENT:FALSE SUMMARY:FDA and CFIA Regulated Goods Webinars DESCRIPTION:Join these 75-minute sessions to learn about the additional requirements and checkpoints that importation of regulated goods undergo. We will introduce you to the processes\, documentation\, notifications\, penalties and responsibilities of the parties involved. Throughout each webinar you will gain a better understanding of the interaction between CBP and FDA for commercial goods destined to the U.S. and CBSA's interaction with CFIA for goods into Canada. Remember\, a customs release does not equal a release for either the CFIA or FDA.\n\n\n\nTopics Include\n\n\n \n \n \n U.S. Food and Drug Administration\n\n \n About the FDA\n Acts and regulations\n Food Safety Modernization Act (FSMA)\n Bioterrorism Act\n Facility registration\n Documentation requirements\n FDA prior notice requirements\n FDA review/exam/sample procedures\n Record keeping\n Customs release process\n Liquidated damages and penalties\n \n \n \n Canadian Food Inspection Agency\n\n \n About the CFIA\n Acts and regulations\n Import licensing\n Import permits\n Documentation requirements\n Wood packaging \n ISPM 15\n Customs release process\n Automated Import Reference System\n Post-entry changes\n Penalties\n \n \n \n \n\n\nWho Should Attend\n\nOwners\, Managers\, Supervisors\, Coordinators and Logistics staff of companies:\n\n\n \n \n \n \n Under review by CBSA or CBP\n Under review by CFIA or FDA\n \n \n \n \n Importing with new staff\n Confused about their additional requirements X-ALT-DESC;FMTTYPE=text/html:

Join these 75-minute sessions to learn about the additional requirements and checkpoints that importation of regulated goods undergo. We will introduce you to the processes\, documentation\, notifications\, penalties and responsibilities of the parties involved. Throughout each webinar you will gain a better understanding of the interaction between CBP and FDA for commercial goods destined to the U.S. and CBSA'\;s interaction with CFIA for goods into Canada. Remember\, a customs release does not equal a release for either the CFIA or FDA.

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\nTopics Include

\n\n\n \n \n \n \n \n \n
\n

U.S. Food and Drug Administration

\n\n
    \n
  • About the FDA
    • \n
  • Acts and regulations
    • \n
  • Food Safety Modernization Act (FSMA)
    • \n
  • Bioterrorism Act
    • \n
  • Facility registration
    • \n
  • Documentation requirements
    • \n
  • FDA prior notice requirements
    • \n
  • FDA review/exam/sample procedures
    • \n
  • Record keeping
    • \n
  • Customs release process
    • \n
  • Liquidated damages and penalties
    • \n
\n 		\n

Canadian Food Inspection Agency

\n\n
    \n
  • About the CFIA
    • \n
  • Acts and regulations
    • \n
  • Import licensing
    • \n
  • Import permits
    • \n
  • Documentation requirements
    • \n
  • Wood packaging \;
    • \n
  • ISPM 15
    • \n
  • Customs release process
    • \n
  • Automated Import Reference System
    • \n
  • Post-entry changes
    • \n
  • Penalties
    • \n
\n
\n\n

Who Should Attend

\n\n

Owners\, Managers\, Supervisors\, Coordinators and Logistics staff of companies:

\n\n\n \n \n \n \n \n \n
\n
    \n
  • Under review by CBSA or CBP
    • \n
  • Under review by CFIA or FDA
    • \n
\n 		\n
    \n
  • Importing with new staff
    • \n
  • Confused about their additional requirements
    • \n
\n
\n LOCATION:Online from any computer or mobile device UID:e.749.4789 SEQUENCE:3 DTSTAMP:20260424T050716Z URL:https://business.swrbot.com/events/details/fda-and-cfia-regulated-goods-webinars-03-16-2016-4789 END:VEVENT END:VCALENDAR