European Production Order definition

European Production Order means a binding decision by an issuing authority of a Member State compelling a service provider offering services in the Union and established or represented in another Member State, to produce electronic evidence;
European Production Order means a decision, issued or validated by a judicial authority of a Member State in application of Article 4(1), (2), (4) and 5, addressed to a designated establishment or a legal representative of a service provider offering services in the Union located in another Member State bound by this Regulation to produce electronic evidence.
European Production Order means a judicial decision which has been issued or validated by a judicial authority of a Member State ('the issuing State') obliging a service provider offering services in the Union and established or legally represented in another Member State bound by this Regulation ('the executing State'), to produce electronic information;

Examples of European Production Order in a sentence

  • The European Production Order and the European Preservation Order are investigative measures that can be issued only in criminal investigations or criminal proceedings for concrete criminal offences.

  • The categories of data that can be obtained with a European Production Order by the competent authorities include subscriber data, access data, transactional data (the three categories commonly referred to jointly as ‘non-content data’) and stored content data.

  • The data ordered through a European Production Order should be provided directly to the authorities without the involvement of authorities in the Member State where the service provider is established or represented.

  • The reasoning with the grounds for the necessity and proportionality of this measure are also part of the European Production Order.

  • The European Production Order is implemented by issuing a European Production Order Certificate (EPOC) (see Article 8), which is translated and sent to the service provider.

  • Suspects and accused Ppersons whose data was soughtobtained via a European Production Order shall have the right to effective remedies against the European Production Order.

  • A European Preservation Order is subject to similar conditions as the European Production Order.

  • The service provider can only be addressed by a European Production Order if it would not be appropriate to address the request to the company, in particular where this would create a risk of jeopardising the investigation, for example where the company itself is under investigation.

  • The European Production Order may only be issued if this is necessary and proportionate in the individual case.

  • Article 5 sets out the conditions for issuing a European Production Order.


More Definitions of European Production Order

European Production Order means a decision ordering the production of electronic evidence, issued or validated by a judicial authority of a Member State in accordance with article 4(1), (2), (4) and (5), and addressed to a designated establishment or to a legal representative of a service provider offering services in the Union, where that designated establishment or legal representative is located in another Member State bound by this Regulation;
European Production Order means a binding decision, issued by a competent authority of a Member State for validation by the competent authority of another Member State compelling a service provider offering services in the Union and established or represented in another Member State, to produce electronic evidence;
European Production Order means a judicial decision which has been issued or validated by a judicial authority of a Member State to have electronic evidence produced by a service provider offering services in the Union and established or represented in another Member State;

Related to European Production Order

  • Cannabis production establishment agent registration card means a registration card that the department issues that:

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Bulk Product means Licensed Product supplied in a form other than Finished Product which can be converted into Finished Product.

  • U.S. Territory means American Samoa, the Commonwealth of the Northern Mariana Islands, Guam, the Commonwealth of Puerto Rico, or the U.S. Virgin Islands.

  • Aerosol Product means a pressurized spray system that dispenses product ingredients by means of a propellant contained in a product or a product's container, or by means of a mechanically induced force. “Aerosol Product” does not include “Pump Spray.”

  • Licensed Fields of Use means the fields of use identified in Appendix B.

  • Final Product means a reasonably homogenous cannabis product in its final packaged form created using the same standard operating procedures and the same formulation.

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • Cannabis production establishment agent means a cannabis cultivation facility

  • Royalty Product means, either (a) an Alnylam Royalty Product, or (b) an Inex Royalty Product.

  • Marihuana-infused product means a topical formulation, tincture, beverage, edible substance, or similar product containing marihuana and other ingredients and that is intended for human consumption.

  • New Product means the Synology-branded hardware product and Synology-branded accessories contained in the original packaging Customer bought from an authorized Synology distributor or reseller. You may see our “New Product” at Product Support Status.

  • Marijuana product means marijuana as defined in 50-32-101 and marijuana-infused products

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

  • Licensed Field means [***].

  • Milk product or "dairy product" means cottage cheese, dry curd cottage cheese, reduced fat cottage cheese, lowfat cottage cheese, cream, light cream, light whipping cream, heavy cream, heavy whipping cream, whipped cream, whipped light cream, sour cream, acidified sour cream, cultured sour cream, half-and-half, sour half-and-half, acidified sour half-and-half, cultured sour half-and-half, reconstituted or recombined milk and milk products, concentrated milk, concentrated milk products, skim milk, lowfat milk, frozen milk concentrate, flavored milk, eggnog, buttermilk, cultured milk, cultured lowfat milk, cultured skim milk, yogurt, lowfat yogurt, nonfat yogurt, acidified milk, acidified lowfat milk, acidified skim milk, low-sodium milk, low-sodium lowfat milk, low-sodium skim milk, lactose-reduced milk, lactose-reduced lowfat milk, lactose-reduced skim milk, aseptically processed and packaged milk, milk products with added safe and suitable microbial organisms, and any other milk product made by the addition or subtraction of milkfat or addition of safe and suitable optional ingredients for protein, vitamin, or mineral fortification. Unless a product is considered a milk product under this subdivision, milk product does not include dietary products, infant formula, ice cream or other desserts, cheese, or butter. Milk products include the following:

  • Licensed Product means a product or part of a product in the Licensed Field of Use: (A) the making, using, importing or selling of which, absent this license, infringes, induces infringement, or contributes to infringement of a Licensed Patent; or (B) which is made with, uses or incorporates any Technology.

  • Adult exploitation means the illegal use of an incapacitated adult or his resources for another's

  • Licensed Territory means worldwide.

  • Regulatory Approval Application means any application submitted to an appropriate Regulatory Authority seeking any Regulatory Approval.

  • Field Order means a written order issued by an authorized County official/employee to the Contractor during construction effecting a change in the Work by authorizing an addition, deletion, or revision in the Work within the general scope of the Work not involving an adjustment in the Contract Price or a change to the Contract Time or Term. No Field Order shall be valid or effective unless it is signed by the County employee(s) who has been authorized in writing by the Chief Executive Officer or his/her designee to execute Field Orders.

  • New Products means any product which is not an Enhanced Product or 2 Existing Product but which is substantially similar to an Existing Product with respect to design and function and possesses reasonable performance improvements. If Company desires to purchase an Enhanced or New Product(s) from Supplier, Company shall so notify Supplier and provide Supplier the opportunity to manufacture such Enhanced or New Product(s), subject to the following conditions and procedures.

  • Royalty-Bearing Product means (a) any Product that is not a Co-Developed Product and (b) any Co-Developed Product to the extent sold outside of the Co-Development Territory.

  • Marketing Approval Application or “MAA” means a New Drug Application (or its equivalent), as defined in the U.S. Food, Drug and Cosmetic Act and the regulations promulgated thereunder, or any corresponding or similar application, registration or certification in any country.