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3-Hour Virtual Seminar on FDA Imports Require Precision in 2019
This Webinar is over| Date | Jul 16, 2019 |
| Time | 11:00 AM EDT |
| Cost | $290.00 |
|
Online
|
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 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.
Event Fee: One Dial-in One Attendee Price: US $290.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com
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 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.
Event Fee: One Dial-in One Attendee Price: US $290.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com
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