Import Licenses Sample Clauses
The Import Licenses clause establishes the responsibility for obtaining and maintaining any necessary import licenses or permits required for the legal importation of goods under the contract. Typically, this clause specifies whether the buyer or seller must secure these documents, and may outline the timing and documentation required to ensure compliance with relevant laws. Its core function is to allocate responsibility and mitigate the risk of delays or legal issues arising from missing or invalid import authorizations.
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Import Licenses. Prior to the date of shipment of the Products, Buyer shall obtain at its sole cost all import licenses and/or other government approvals that may be required by the country of importation. Upon ▇▇▇▇▇▇’▇ request, Buyer shall provide ▇▇▇▇▇▇ with copies of such import licenses and/or government approvals to evidence Buyer’s compliance with this provision. Buyer represents and warrants that it is not, and Buyer shall not, directly or indirectly, transfer the Products to, a person or entity listed as: (1) a Specially Designated National or Blocked Person by the U.S. Treasury Department; (2) a Denied Person by the U.S. Commerce Department; (3) a Denied Entity by the U.S. Commerce Department; or (4) a Debarred Party by the U.S. State Department. Buyer shall indemnify, defend and hold ▇▇▇▇▇▇ harmless from any claim, loss, damage, fines, penalties, liability or expense incurred with regard to Buyer’s failure to comply with this provision.
Import Licenses. Where the Products are being delivered to a Delivery Location outside of the United States, you are responsible for obtaining any necessary import licenses or permits necessary for the entry of the Products into any non-US territory.
Import Licenses. With IMED's reasonable assistance in respect to the execution of documents and other ministerial actions, DEBIOTECH shall cooperate as reasonably necessary to enable IMED to procure and maintain all licenses reasonably necessary to ship Products and Accessories from the point of manufacture to IMED in accordance herewith. DEBIOTECH shall comply with, and IMED agrees to inform DEBIOTECH of any change in, to the extent IMED is aware or has been made aware of, all other laws, regulations and governmental directives relating to the import of technical data, goods and services including, without limitation, those enforced by the United States Departments of Commerce and Defense and shall not permit the Products and Accessories to be manufactured in a manner or with any component, or involving any jurisdiction, so that it may not lawfully be imported into the Territory.
Import Licenses. Distributor shall obtain import and reexport licenses and permits and take all other actions required in connection with the import or reexport of Products purchased hereunder.
Import Licenses. To the extent import licenses are required for the importation of the Products into the Territory, Agent hereby agrees that it will be responsible for securing and maintaining such import licenses. Payment of all fees and expenses associated therewith shall be the responsibility of Principal.
Import Licenses. To the extent import licenses are required for the importation of the Products or Sales Aids into the Territory, NSUSA hereby agrees that it will be responsible for securing and maintaining such import licenses and payment of all costs and expenses associated therewith.
Import Licenses. The sole responsibility far obtaining any required import licenses or any other related license or documentation shall rest with BUYER.
Import Licenses. The sole responsibility for obtaining any required import licenses or any other related license or documentation shall rest with BUYER. [***] Confidential information has been omitted and filed separately with the Securities and Exchange Commission pursuant to a confidential treatment request.
Import Licenses. Exchange Controls, and Other Governmental Approvals, Compliance.
6.4.1 Merck shall, at its own expense: (a) obtain any registration, license, permit, governmental approval (collectively, any "registration") that may be necessary to permit the purchase, distribution and resale by Merck of the Testing Device and the Reader in each country in the Territory; (b) comply with all registration requirements for each country in the Territory; and (c) comply with any and all laws, regulations and orders that may be applicable to Merck by reason of its execution of the Agreement, including any requirement to be registered as Biosite's independent distributor with any governmental authority, and including any and all laws, regulations or orders that govern or affect the ordering, export, shipment, import, sale (including government procurement), delivery, or redelivery of the Testing Device and the Reader in the Territory. Merck shall not engage in any course of conduct that, in Biosite's reasonable belief, would cause Biosite to be in violation of the laws of any jurisdiction.
6.4.2 All registrations in the Territory of the Testing Device and the Reader shall be made in the name of Merck and shall remain the property of Merck during the term of the Agreement. Merck shall provide Biosite a copy of each such registrations and application therefor.
6.4.3 Upon the expiration or earlier termination of the Agreement, Biosite shall have the right, at its option, to take over the above-described registrations or, where necessary, to obtain registration under Biosite's name at its own cost. Merck shall use its best efforts to assist Biosite in the transfer to, or obtaining of any such registrations in the name of, Biosite (or Biosite's agent) in a quick and efficient manner.
Import Licenses. With respect to any import laws and other regulations of the country of destination and its various cognizant departments regarding the import of the Products hereunder, Buyer shall be solely responsible for obtaining and complying with any and all import licenses or other authorizations which may be required for importing the Products.