FDA offers New Import Program for 2017

MessageThis Webinar is over
Date Jun 20, 2017
Time 10:00 AM
Cost $150.00
FDA offers some relief from the strict requirements if you participate in a voluntary Affirmation of Compliance (AOC). Providing accurate information is necessary in order to reconcile the PREDICD, ACE, Invoice and AOC information.

Why should you Attend:
The new import entry filing requirements became effective in 2016 and are posing problems for user. Failure to provide the correct information creates costly delays and, in some cases, the frustrating task of contacting the FDA to resolve the problem.

Areas Covered in the Session:
    FDA's required information for the PREDICT software screening prior to entry
    FDA product codes
    Custom's required information for the ACE software system prior to entry
    Custom's Harmonized Tariff Schedule (HTS)
    Affirmation of Compliance (AOC)

Who Will Benefit:
    Business Planning Executives
    Regulatory Managers
    In-house Legal Counsel and Contract Specialists
    Venture Capitalists
    Business Acquisition Executives

Speaker Profile:
Casper (Cap) Uldriks, through his firm “Encore Insight LLC,” brings over 32 years of experience from the FDA. He specialized in the FDA’s medical device program as a field investigator, served as a senior manager in the Office of Compliance and an Associate Center Director for the Center for Devices and Radiological Health.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com


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