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The FDA’s is making major changes to its import program. Some changes start this year. They affect all FDA regulated products. You can voluntarily participate and reap cost savings. The FDA has integrated its import program into the Automated Commercial Environment program, but you must understand information-reporting requirements or you will miss the boat, literally. The FDA also offers a new pre-qualification program for food products. Are you ready to apply? Will you be accepted? If you qualify, you may participate in an expedited clearance process that is similar to the TSE-pre-check for air travel or Homeland Security’s Global Entry Program for international travelers.

Import requirements and procedures for the FDA are integrated into the U.S. Customs and Boarder Patrol entry process. You need to understand how their integrated programs and legal requirements work. It is surprisingly seamless. When products are detained, the entry becomes a very costly problem. Firms need to know what its options are and how it can resolve a detention.

Learning Objectives:
FDA’s new cost-saving import programs
Understand how U.S. Customs and FDA legal requirements intersect
Know how to manage foreign suppliers
Understand FDA’s internal procedures
Learn how to mitigate and resolve import detentions

Who will Benefit:
The FDA’s regulatory controls for imported and exported devices have become increasingly pervasive and stringent. Foreign manufacturers, foreign exporters and domestic initial importers face greater scrutiny and are subject to expensive consequences if they do not plan carefully. Attendees need to understand the FDA’s and the US Customs Border Patrol’s regulatory criteria, inter-agency agreements and intra-agency procedures. The conference provides attendees with the opportunity to understand their work’s inter-relationship with other attendees’ roles.

Business Planning Executives
Regulatory Managers
In-house Legal Counsel and Contract Specialists
Venture Capitalists
Business Acquisition Executives

Use coupon code NB5SQH8N and get 10% off on registration.

For Registration:

Not sure if you want to exhibit at or attend the FDA's Import Program for 2016 - New Pathways and Pitfalls? See the panels below to get the information you need to make an informed decision.

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Conference/Event Dates: 11/17/2016 - 11/18/2016
Conference/Event Hours: 8:30 AM - 4:30 PM
Classification: B2B
Primary Industry: Sciences
Other Industries: Business, Sciences
Estimated Attendance: 30
Cost to Attend: One Registration - $1699
Audience: Business Planning Executives
Regulatory Managers
In-house Legal Counsel and Contract Specialists
Venture Capitalists
Business Acquisition Executives
Owners of New or Developing Import/Export Firms
International Trade Managers
Import Brokers
Venue: Courtyard Boston Cambridge
Venue Phone: (888) 717-2436
Venue Type: Indoor - Hotel
Show Owner:ComplianceOnline

Booth Size Booth Cost   Available Amenities
Call for information.   Electricity: n/a
  Water: n/a
  Generator: n/a
  Marketing Vehicles Allowed: Call
Other Booth Sizes Available: n/a

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