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    FDA COMPLIANCE AND CFIA TRAINING IN REGULATORY CHA 2017 - FDA & CFIA 2016 Regulatory Changes/Updates -By AtoZ Compliance

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    Website https://www.atozcompliance.com/trainings-webinar/cross-industry-functions/trade-and-logistics/compli | Want to Edit it Edit Freely

    Category Medical Device;Healthcare;Quality Control

    Deadline: February 16, 2017 | Date: February 16, 2017

    Venue/Country: Online, U.S.A

    Updated: 2017-01-17 17:45:39 (GMT+9)

    Call For Papers - CFP

    Key Take Away :

    This webinar will cover the 2016 regulatory changes and updates for the FDA(US Food and Drug Administration) compliance programs and the CFIA (Canadian Food Inspection Agency) since 2016 is a banner year for updates and changes for both agencies.

    Overview :

    The US FDA regulatory compliance training and Canada’s CFIA training have moved from paper based reporting to each countries’ respective single window system. Many of the old forms have been replaced with electronic formats.

    The FDA is requiring all foreign food based businesses to re-register, and Health Canada has many changes as well.

    Learn what you need to update your business and keep up with all the new changes.

    Why Should You Attend :

    The webinar will cover the changes the USFDA is putting in place to report through Customs ACE reporting tool. It will cover the Canadian GMO rules. What do these agencies have in common and where do they differ? This can save companies from duplicating internal restrictions and possible violations from assumptions.

    The webinar will cover a brief history of both agencies. What is the mission of each agency, do they differ?Are there new restrictions for importing and exporting? Determine if new labelling requirements will affect your products. What authority do these agencies have and how can they enforce regulations?

    The webinar will cover new and updated product code classifications as well as recall protocol. Staying ahead of changes can keep you compliant and your business’s reputation clean. What’s next for these agencies? Determine if your current compliance programs are sufficient. New requirements and regulations can keep you scrambling, this webinar will help you stay ahead of the game.

    Areas Covered In This Webinar :

    The latest regulatory changes and requirements

    Learn the latest terminology and acronyms

    How does this affect global trade facilitation?

    Determine current risk level and how to remain compliant

    Learn the latest product marking requirements

    Determine if your medical devices are marked and registered compliantly

    Changes from June, July, August, and upcoming important dates

    Learning Objectives :

    Understanding the latest changes and legal requirements

    Understand when changes and reporting requirements become mandatory

    Determine software updates, availability, and requirements

    Product marking and registration requirements

    Identify other governmental agency requirements

    Learn what reports are available

    Learn how your broker, forwarder, and legal counsel can help

    Who Will Benefit :

    Internal regulatory departments

    Validation specialists

    Documentation specialists

    Quality control professionals

    Medical devices professionals

    FDA professionals

    Finance professionals

    Global tax professionals

    Trade compliance professionals

    Logistics managers

    Company compliance officers

    Import/export professionals

    Global trade professionals

    Brokers and forwarders

    Professionals who are looking for risk reduction, time and cost savings

    Companies engaged in global trade

    For more information, please visit : https://www.atozcompliance.com/trainings-webinar/cross-industry-functions/trade-and-logistics/compliance-in-fda-and-cfia-2016-regulatory-updates-and-changes/grant-smith/300204

    Email: supportatatozcompliance.com

    Toll Free: +1- 844-414-1400

    Tel: +1-516-900-5509

    Level:

    Intermediate

    Speakers Profile :

    Grant Smith

    Grant Smith an International trade consultant is the owner of Grant Smith Consulting, LLC. Mr. Smith is a trade compliance professional with 30 years of experience in global logistics and trade compliance.

    A licensed customs broker and certified customs specialist, Mr Smith is also IATA and DOT Certified. He has been working for global corporations, implementing trade programs and providing training in multiple regions internationally.


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.