Two Day Seminar on the FDA's New Import Program for 2017: Strict Precision (Boston, MA, United States - November 9-10, 2017) - Research and Markets

DUBLIN, May 26, 2017 /PRNewswire/ --

Research and Markets has announced the addition of the "FDA's New Import Program for 2017 - Strict Precision" conference to their offering.

The FDA continues to change its import program to better manage new problems and to use new procedures to make the whole process easier.

The FDA and U.S. Customs and Border Protection (CBP) are relying more and more on computer programs to expedite the import process. When and how you use these programs can make a big difference in the net profit derived from even a single shipment. The new Voluntary Qualified Importer Program (VQIP) is one such example.

Another example is CBP's and FDA's implementation of the Automated Commercial Environment (ACE) program, which will become mandatory for importers in 2016. If you fail to correctly use new import procedures and programs, you will be operating under an expensive disadvantage.

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
- Learn how to avoid common problems
- Develop practical ways to improve your import and export business
- You will be able to answer the following questions with this course without saying, I don't know?
- What are the FDA's import legal requirements and policy?
- How do you deal with the FDA and the U.S. Customs and Border Patrol procedures?
- What happens when your product is detained?
- What happens if a foreign manufacturer is in trouble with the FDA?
- How do you inter-act with the FDA to work out problems?
- Why are import and export rules different or does it even matter?

Topic Background:

FDA's import and export program is complex and keeps changing. The FDA's and the U.S. Custom's new import and enforcement program operates with a streamlined computer system and can leave firms at a loss to understand the short term and long term effects of a detained shipment. The law now requires foreign firms to register and submit specific information to enter U.S. commerce.

Foreign establishments are subject to FDA inspections and quality testing. Failing either FDA activity typically prevents a foreign firm's product from entering U.S. commerce. If product is detained, resolving the problem with FDA is time consuming, expensive and uncertain. Without an adequate or informed approach to your import program, the specialized federal government process and roadblocks can seem impossible to overcome. To compound the problems, working with foreign establishments presents inherent difficulties based on cultural differences business practices and language barriers.

Other foreign and domestic and legal requirements intersect with FDA's import and export program, some for the better, some not. For example, not all foreign firms are treated the same under the FDA's law. A clear example is the FDA's uses of automatic detention based on the country of origin, type of product or an establishment's history. With the growing use of off-shore operations, managing imported products can and does present obvious and hidden problems.

Agenda:

Day 01(8:30 AM - 4:30 PM)

08.30 AM - 09.00 AM: Registration

09.00 AM: Session Start

Day 1 - Morning

FDA's legal requirements

- Statutory authority
- Regulations

Foreign manufacturers obligations

- U.S. initial importers obligations
- User Fees
- How does FDA do its job
- What is CPB and how do they do their job

Selecting foreign suppliers

- Inspection history
- Samples analyzed
- Vendor Audit

Day 1 / Afternoon

Product Import Procedures

- Entry Process (U.S. Customs/FDA)
- How to Pick the right Custom House Broker
- Documentation

- FDA Form 2877
- CPB Form 3461
- Medical Device Affirmations of Compliance (AofC)
- Electronic Entry Filing- FDA's PREDICT computer screening program
- U.S. Customs Automated Commercial Environment (ACE) program
- Product sampling / testing
- Detention, block list, automatic detention

- Quality standards
- Country of origin
- Product type

(Case Study)

Day 02 (8:30 AM - 4:00 PM)

Day 2 / Morning

Detention

- Options for a detained shipment
- Negotiating with FDA and U.S. Customs

- What to say
- What not to say
- When to give up

- Release from Detention and Government Refusal Remedies
- Reducing the risk of detention

(Group study for mitigating detention risks)

Day 2 / Afternoon

Enforcement

- U.S. Customs and FDA authority
- Burden of proof
- Assistant U.S. attorney
- Government remedies

Special provisions

- Counterfeit
- Import for export
- International trade shows
- Investigational device
- Compassionate Use

For more information about this conference visit http://www.researchandmarkets.com/research/2svcpn/fdas_new_import

Media Contact:

Laura Wood, Senior Manager
[email protected] 

For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

U.S. Fax: 646-607-1907
Fax (outside U.S.): +353-1-481-1716

SOURCE Research and Markets

Related Links

http://www.researchandmarkets.com