Thursday, February 16, 2012

U.S. Customs & Border Protection Seized My Goods - Oh No!


U.S. Customs & Border Protection (CBP) seizes merchandise EVERY day (and there is a LOT you can do to get your merchandise back!).  Check out the latest 2011 stats on intellectual property rights enforcement and seizure statistics.

What some don't know is the merchandise does NOT even have to be destined for the U.S. for CBP to seize it.  Yes, it's true.  CBP detains and physically inspects cargo daily. CBP is supposed to issue timely detention notices and the detention notices are supposed to include the specific reason for the detention, anticipated length of the detention; nature of the tests or inquiries to be conducted; and nature of any information which, if supplied to U.S. Customs may accelerate the disposition of the detention.  I wish I had a dollar for every importer that told me they never received one, or where the rationale for detention was blank, or said IPR (intellectual property rights)!

Tuesday, February 14, 2012

HOW TO GET OFF THE FDA BLACK LIST (Import Alert List)


What is the Black List?

The United States Food and Drug Administration (FDA) has authority from Congress to place an importer, manufacturer, shipper, grower, geographic area, or country on a “detention without physical examination” (DWPE) list (aka the FDA’s black list). To check if a company you are doing business with is on such a list, check FDA’s Import Alert page, you can search by country, company, etc. If your company is on this list, any merchandise you import may be detained as soon as it is offered for entry into the United States. You will have to prove to the FDA that the merchandise should be allowed to enter the U.S., otherwise, it will be refused entry and must be exported or destroyed within 90 days. The company/country, etc. will remain on this black list, until information is presented to the FDA that proves the merchandise is no longer violative.

How to Get Off the Black List

Thursday, February 9, 2012

Do You Know the TOP 10 COMPLIANCE TIPS?

If you import, you need to!

On behalf of the Organization of Women in International Trade (OWIT-South Florida), I am hosting an informal round table where members OWIT will have the opportunity to get to know one another and learn all about compliance with U.S. Customs and Border Protection (CBP)!

Yes, men are welcome!

This session is especially important for importers and brokers and those in involved in international trade.

Attendees will receive a special "cheat sheet" providing great resources to utilize when importing, including the top 10 compliance tips.

Space is limited to OWIT members! Become a member of OWIT here (it is only $100 for a YEAR of benefits including these FREE IBR's), and assure your spot by sending in your RSVP today!

Please email Jennifer Diaz with any questions!


Wednesday, January 11, 2012

Importing into the United States in Compliance with U.S. Customs & Border Protection (CBP)

Do you want to learn the Top 10 Tips When Importing to Ensure Compliance?  What about the Importance of CBP Rulings for Classification, Valuation and Country of Origin?

How about Cost Savings practices like utilizing Free Trade Agreements?

Well you can learn this and hot topics like:

- Importance of protecting Intellectual Property Rights

- Basic customs concepts and terms

- What to do if you encounter a CBP detention and/or seizure case

- Learn when to submit a Prior Disclosure to CBP

Join my webinar with Compliance Online, January 27, 2012, at 1:00 pm eastern. 

You can join the live session and ask questions! 

If you import merchandise into the U.S., you may not realize, but, you are the responsible party! In this presentation, we will discuss how to comply with U.S. Customs and Border Protection’s (CBP) vast laws and regulations. By the end of the Seminar you will know and understand the importance of tariff classification, Customs valuation, Country of origin marking, intellectual property rights and Free Trade Agreements. You will also learn basic customs concepts and terms like CBP Form 3461 & CBP 7501, Protests, Seizure cases, Liquidated damage claims, Penalties/Fines, Prior disclosure, and FP&F Petition Process.

Thursday, December 22, 2011

CBP Commissioner Bersin Tenders Resignation Effective December 30

Customs and Border Protection (CBP) Commissioner Alan Bersin has announced his resignation effective December 30. Deputy Commissioner David V. Aguilar is slated to serve as Acting Commissioner.

In a statement announcing his resignation, Bersin said he was grateful for the chance to lead CBP.

"My service as commissioner has been one of the most rewarding experiences of my public life," Bersin said Thursday. "I am immensely proud of the significant and meaningful achievements we have made on our borders and at our nation's ports of entry over nearly two years."
Bersin's recess appointment term expires Dec. 31.

Will YOUR Tariff be Changed in the 2012 Update??

One way to find out!

CSMS #11-000317, dated December 21, 2011, advises brokers that the 2011/2011 Harmonized Tariff Schedule of the United States (HTSUS) will contain many changes. 

Specifically, the notice states:

To: Automated Broker Interface
Harmonized System Update (HSU) 1108 was created on December 20, 2011 and contains 577 ABI
records and 118 harmonized tariff records.

Changes were made as a result of the 484 (F) Committee. The Committee for the Statistical Annotation of the Tariff Schedules mandated modifications effective January 1, 2012.

As always, these changes will be included in the 2012 USHTS. However, at this time, please contact your client representative for questions regarding specific records.

Adjustments required by the verification of the 2011 Harmonized Tariff Schedule (HTS) were made as well.

The modified records are currently available to all ABI participants and can be retrieved electronically via the procedures indicated in the CATAIR. For further information about this process, please contact your client representative. For all other questions regarding this message, please contact Jennifer Keeling via email at Jennifer.Keeling@dhs.gov.
The prelimary 2012 HTSUS is out!  Time to check your tariffs for the new year.

Did your tariff change?

Friday, December 16, 2011

NEW CBP Technology To Increase Efficiencies at Port Miami

NEWS BLAST! 

U.S. Customs and Border Protection (CBP) is set to launch Enforcement Link to Mobile Operations (ELMOcargo) at the Port of Miami. This technology will allow CBP Officers and Agriculture Specialists to release inspected cargo in real-time.

Currently, CBP Officers and Agriculture Specialists conduct inspections on site, but the subsequent release of cargo is delayed until field personnel return to the office and enter inspection results into their data systems.

With the implementation of ELMOcargo, field officers using handheld devices will be able to immediately clear containers. This device speeds up release time by up to four hours making operations more efficient while continuing to keep the Port secure.

CBP Agriculture Specialist recently started using this new technology as a pilot at other Florida ports and agreed to expand the program to Port Miami starting in January 2012.

About the Port of Miami
The Port of Miami is among America's busiest ports and recognized across the globe with the dual distinction of being the Cruise Capital of the World and the Cargo Gateway of the Americas. The Port of Miami contributes more than $18 billion annually to the South Florida economy and helps provide direct and indirect employment for more than 180,000.

MEDIA CONTACT:
Andria C. Muñiz
305-347-4962
amuniz@miamidade.gov

Wednesday, October 5, 2011

33 Interesting and Exciting Career Paths in International Business!

We often come across great resources we want to share with others... This is exactly what this post is all about!

I was sent 33 Interesting and Exciting Career Paths in International Business and thought MANY of you could benefit from this.

I hope this is beneficial for you!

Monday, August 15, 2011

10th Annual IBWOY Awards - November 1, 2011 - SAVE THE DATE!!!

On November 1, 2011, the Organization of Women in International Trade's South Florida will host our 10th Annual International Business Women of the Year (IBWOY) Awards (men are absolutely welcome)!

This is my final year as President of OWIT-South Florida, making this IBWOY awards that much more special to me. I hope you will be there to join in this truly exceptional event as we honor 3 outstanding international business women who are helping pave the way for future women leaders.
  • WHO:       The Organization of Women in International Trade  
  • WHAT:     10th Annual International Business Women of the Year (IBWOY) Awards
  • WHEN:      November 1, 2011, 11:00 am - 2:00 pm
  • WHERE:   The InterContinental Miami West Hotel - Doral, 2505 North West 87th Ave. Miami, FL 33172
  • COST:       Early Bird (register by Sept. 16): $50 members/$65 non-members  Regular/Event Day Registration:  $75 members/$85 non-members Table of ten (10): $500
In addition to our awards portion, we have a silent auction where we donate proceeds to International Business Students in local universities, as part of National Scholarship Month (last year we raised $4,000!). If you have an item to donate, we would be grateful to receive it, please let me know! We also have great sponsorship opportunities, tables for IBWOY are only $500, ($50/ticket as opposed to $65/ticket for non-members). Take advantage of early registration fees as well! ($50/member, $65/non-member until September 16, thereafter, $75/member, $85/non-member).

Let's celebrate a decade of women in international trade together on November 1, 2011!!
RSVP today!

Monday, August 8, 2011

Gluten Free Labeling is Coming - But, First, FDA Wants to Hear From YOU!!!!

Imagine a world where a manufacturer’s claims that their products are “gluten free” could be trusted by U.S. consumers.  Imagine a world where U.S. consumers were promised a definition of “gluten free” by the U.S. Food and Drug Administration (FDA), and the FDA held all manufacturers and importers to the same stringent standard….

Good news, we’re getting close!!

As of August 2, 2011, FDA has re-opened the comment period so that they can hear from YOU.  Yes, YOU!  FDA wants to hear from Celiacs, gluten sensitive consumers, et al. in the U.S.  Why, you ask?  Well, the FDA is firming up their definition of “gluten free”; and wants to know that the gluten free community is satisfied with the FDA’s finalized definition.  So, let’s make sure we tell the FDA what's important to us.  FDA has proposed a definition of "gluten free" in order for the term to be used on labeling of food products.

FDA’s proposed rule defines “gluten free” as products that do not contain:
  1. an ingredient that is any type of wheat, rye, barley, or crossbreeds of these grains
  2. an ingredient derived from these grains and that has not been processed to remove gluten
  3. an ingredient derived from these grains and that has been processed to remove gluten, if it results in the food containing 20 or more parts per million (ppm) gluten
  4. 20 ppm (parts per million) or more gluten
FDA wants to hear from the public and industry. The public comment period on the proposed rule will officially open after noon on Aug. 3, 2011, and will remain open for 60 days (until October 3, 2011). FDA prefers electronic comments, go to http://www.regulations.gov/ and
  1. choose “Submit a Comment” from the top task bar
  2. enter the docket number FDA-2005-N-0404 in the “Keyword” space
  3. select “Search”
FDA’s Center for Food Safety and Applied Nutrition (CFSAN) is tasked with making this happen, check out FDA's webpage which shows the safety assessment done to confirm 20 ppm is the correct standard to use.   

FDA held a conference call with industry, where the FDA allowed questions on opening up the comment period, and hopefully bringing truthful gluten free labeling to U.S. consumers soon.  Some questions asked where the methods in which FDA would test manufacturer’s products (answers were the Elisa R5 Mendez method, and Morinaga Method (currently used by the Japanese government for allergen labeling).  Presently, the Food Service and Products industry doesn't have to use these methods, but these are the methods FDA will use for enforcement.  

FDA is well aware that 20 ppm may not protect everyone, FDA wants your comments on this issue, what would truthful gluten free labeling be to you??  I was thinking about a range, 0-5 ppm, 5-10 ppm, 10-15 ppm, etc. to be included with “gluten free.”  FDA was also thinking about low/very low gluten labeling – but, what would be considered low?  What would be low or very low to you?  Tell the FDA!!
As far as timing goes, FDA will review the comments received, and is targeting the 3rd quarter of 2012 to publish a final rule.   

Yours truly asked the FDA about enforcement because I want to know how FDA will check on these products once these standards are implemented.  FDA advised there will be a compliance program set with the new rule, which will likely entail inspections, label review, (although I was hoping to hear about more lab testing of products).  Further, I asked about the size of FDA’s budget to assist in enforcement (once we all agree on definitions and a final rule comes to be…) but, there was no comment from the FDA on the budget to enforce (only a chuckle...).

We all think of the monsters out there who have preyed on Celiac’s/gluten free consumers, and did not in fact sell a gluten free product.  FDA will issue warning letters, seize products, issue injunctions, issue mandatory recalls, etc., when faced with manufacturers who are selling gluten free product that is NOT truly gluten free.
Let’s get to it, let’s tell the FDA you agree with 20 ppm, don’t agree, want low/very low standards (explaining what your tolerances are), or whatever your prospective may be.  FDA is listening, they want to hear from you, speak now!  You have until October 3 to have your voice heard before the final rule, and then, the hope is you will trust the products on your shelves that state, “gluten free”.