FDA offers New Import Program for 2017

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Category Annual Product Quality Review, Manufacturing, Risk, Pharmaceutical Webinars, manufacturing technology, industrial manufacturing, industrial manufacturing industry, Regulatory Affairs Managers

Deadline: June 18, 2017 | Date: June 20, 2017

Venue/Country: Online, U.S.A

Updated: 2017-04-24 18:45:18 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com