FDA's New Import Program for 2019

Overview:In this interactive session author will discuss about the FDA's required information for the PREDICT software screening prior to entry and Custom's Harmonized Tariff Schedule (HTS).
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 entryFDA product codesCustom's required information for the ACE software system prior to entryCustom's Harmonized Tariff Schedule (HTS)Affirmation of Compliance (AOC)
Who Will Benefit:Business Planning ExecutivesRegulatory ManagersIn-house Legal Counsel and Contract SpecialistsVenture CapitalistsBusiness 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.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14@gmail.com