By acceptance of the order, the supplier undertakes active steps to inform the client about classifications for the products to be delivered.
The duty to provide information includes the communication of the respective classification in accordance with the EC-Dual-Use-regulation 428/209, the U.S.(Re-)Export Control law (EAR) and EC regulation 1277/2005 (drug precursors), with corresponding notes in the delivery documents (order acknowledgement, delivery note, invoice, etc.) and before the shipment to the following office:
Team Export Control
At the request of the client the supplier obligates to provide all other necessary information regarding our compliance (f.e. our Export Control declaration).
The contact office listed above should be informed immediately in the event of any changes to the product classification.