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

Overview: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.
Why should you Attend: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 proofFDA registration, product information and the PREDICT screening programSubmitting information before cargo arrival in the U.S.FDA"holds," "detentions" and what to do immediately
Who Will Benefit:Regulatory Affairs DirectorsSoftware Designers/Specification DevelopersProduction ManagersQuality Assurance DirectorsIn-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.
Event Fee: One Dial-in One Attendee Price: US $290.00
Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14@gmail.com