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U.S. Department of Commerce Imposes Preliminary Tariffs on Chinese Solar Products

On June 3, 2014, the U.S. Department of Commerce (DOC) announced its preliminary determination in the countervailing duty (CVD) investigation of crystalline silicon photovoltaic products (“solar products”) from China. DOC...more

6/6/2014 - China Countervailing Duties Customs and Border Protection Exports Investigations Photovoltaic Solar Products Tariffs U.S. Commerce Department

Iran Sanctions Relief Offers Limited Opportunities and Substantial Risks

Introduction and Summary - On January 20, 2014, the departments of State and the Treasury announced details of the United States’ plan to suspend certain sanctions against Iran pursuant to the November 24, 2013 Joint...more

1/29/2014 - Department of State EU Foreign Policy Iran Iran Sanctions Middle East U.S. Treasury

U.S. Subsidiary of SolarWorld Files New AD/CVD Petitions on Chinese-Origin Solar Cells

On December 31, 2013, SolarWorld Industries America, Inc. (“SolarWorld”) – the U.S. subsidiary of Germany-based SolarWorld AG – filed petitions for the imposition of antidumping and countervailing duties (AD/CVDs) on...more

1/3/2014 - Antidumping Duties China ITC Solar Energy Solar Panels U.S. Commerce Department

U.S. Department of Commerce Soon to Launch Review of Duties on Chinese-Origin Solar Cells amidst Challenges to Scope of Coverage...

December 2013 will mark the first “anniversary month” of the antidumping (AD) and countervailing duty (CVD) orders on Chinese-origin crystalline silicon photovoltaic (PV) cells, whether or not assembled into modules. The U.S....more

11/21/2013 - Antidumping Duties China Solar Energy Solar Panels Trade Policy U.S. Commerce Department

Bringing a Medical Device to Market in the United States

Is the Product a Medical Device? The first consideration in bringing a medical device to market in the United States is to confirm that the product in question is actually a medical device. The U.S. Food and Drug...more

7/22/2013 - Medical Devices

Medical Device Postmarket Compliance in the United States

Introduction - Once the U.S. Food and Drug Administration (FDA or “the agency”) has cleared or approved a medical device for marketing in the United States, there are still significant postmarketing requirements with...more

7/22/2013 - FDA Labeling Manufacturers Medical Devices

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