3-Hour Virtual Seminar on FDA Imports Require Precision in 2019


Tuesday, July 16, 2019   |   09:00 AM PST | 12:00 PM EST   |   Duration: 3 Hours          

Live

One Dial-in One Attendee

Price: US$290.00


Corporate Live

Any number of participants

Price:US$490.00


Duration: 3 Hours  

Recorded

Access recorded version,
only for one participant ?

Price: US$340.00

Corporate Recorded

Access recorded version,
Any number of participants ?

Price: US$540.00

After attending this 3-Hour Virtual Seminar, you will have great understanding of how FDA and Customs and Border Protection (CBP) operate a joint program.
Casper Uldriks   Product Id : 502338
  Instructor : Casper Uldriks

  More Trainings by this Expert


Overview:

Importing FDA regulated products requires careful planning before you even start. Registration, product compliance, record and data submission must be exactly correct, or else, FDA's entry requirements with detain your product. Some mistakes are common, others reflect a lack of understanding of how FDA and Customs and Border Protection (CBP) operate a joint program.

Correcting problems can cost you time and money, especially when you do not work promptly with the FDA. If you end up with having your entry "refused." There is no appeal. Then you face the possibility of additional steep fines by CBP.

Why should you Attend: Firms typically run aground with importing FDA regulated products because they do not understand how to prepare, conduct and report in accord with FDA requirements. If the exporter and importer do not follow the procedures or fail to submit correct information, the road forward has an expensive and time-consuming toll. A failure to do things correctly will create a "bad actor" image, which is very hard to undo and FDA does not forget, somewhat like a regulatory elephant.

If you understand FDA's and CBP's import program, your business can operate in a competitive way. If you do not, your customers, foreign suppliers, stockholders will see the consequences and not be forgiving.

Areas Covered in the Session:

  • FDA's legal authority and burden of proof
  • FDA registration, product information and the PREDICT screening program
  • Submitting information before cargo arrival in the U.S.
  • FDA"holds," "detentions" and what to do immediately

Who Will Benefit:
  • Regulatory Affairs Directors
  • Software Designers/Specification Developers
  • Production Managers
  • Quality Assurance Directors
  • In-house Legal Counsel


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. He developed enforcement actions and participated in the implementation of new statutory requirements. His comments are candid, straightforward and of practical value. He understands how FDA thinks, how it operates and where it is headed. Based on his exceptionally broad experience and knowledge, he can synthesize FDA's domestic and international operational programs, institutional policy and thicket of legal variables into a coherent picture. Professional credentials: JD - Suffolk University, licensed in Massachusetts and the District of Columbia; M.Div in psychology - Boston University with internship through Harvard University.




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