FDA's Import Program for 2016 - New Pathways and Pitfalls

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Category FDA Compliance;

Deadline: December 10, 2015 | Date: December 10, 2015-December 11, 2015

Venue/Country: Philadelphia, U.S.A

Updated: 2015-11-20 21:27:35 (GMT+9)

Call For Papers - CFP

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

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/fdas-new-import-program-concerning-international-consequences-seminar-training-80133SEM-prdsm?channel=ourglocal