Mexican Regulatory Approval definition

Mexican Regulatory Approval. ’ means the issuance of an authorization by Cofece to Agnico Eagle and Cayden to consummate, on terms satisfactory to Agnico Eagle, the transactions contemplated by the Arrangement Agreement, or the expiry of the relevant statutory term (and any extension thereof) prescribed by the Federal Economic Competition Law (Mexico) (Ley Federal de Competencia Econo´mica) without a decision by Cofece, and the deemed authorization of Agnico Eagle to consummate the transactions contemplated by the Arrangement Agreement.
Sample 1
Mexican Regulatory Approval means the issuance of an authorization by Cofece to AuRico and/or Alamos, as applicable, to consummate, on terms satisfactory to AuRico and/or Alamos, as applicable, the transactions contemplated hereby, or the expiry of the relevant statutory term (and any extension thereof) prescribed by the Federal Economic Competition Law (Mexico) (Ley Federal de Competencia Económica) without a decision by Cofece, and the deemed authorization of AuRico and/or Alamos, as applicable to consummate the transactions contemplated by the Arrangement Agreement; - 125 -
Sample 1
Mexican Regulatory Approval means the issuance of an authorization by Cofece to AuRico and/or Alamos, as applicable to consummate, on terms satisfactory to AuRico and/or Alamos, as applicable, the transactions contemplated hereby, or the expiry of the relevant statutory term (and any extension thereof) prescribed by the Federal Economic Competition Law (Mexico) (Ley Federal de Competencia Económica) without a decision by Cofece, and the deemed authorization of AuRico and/or Alamos, as applicable to consummate the transactions contemplated hereby;
Sample 1

Examples of Mexican Regulatory Approval in a sentence

  • Notice of the waiver of the Mexican Regulatory Approval Condition was given by the Offeror to the Depositary on October 17, 2005.

  • It is anticipated that MMI will be responsible for manufacturing and supplying the Myostatin(TM) Blocker product to Pilgrim's Pride to perform any required research and trials to obtain Mexican Regulatory Approval; PROVIDED HOWEVER, that the provision of such product by MMI to Pilgrim's Pride shall be conditioned upon such product being available in sufficient quantities to honor all of MMI's current commitments under all of MMI's existing license agreements for the United States.

  • Spreadsheet identifying AT&T Wireless Proposed Use of Pineland Facilities.

  • It is anticipated that MMI and Pilgrim's Pride will formulate a committee of managers which will develop protocols for the commercial-scale production and sale of products based on the Myostatin(TM) Blocker Technology in the country of Mexico (the "Mexican Regulatory Approval").

  • It is anticipated that MMI will grant the Limited License to Pilgrim's Pride for the limited purposes of: (1) performing any required research and trials to be conducted in their effort to obtain Mexican Regulatory Approval and (2) for use of the Myostatin(TM) Blocker technology limited to improving chicken meat production economies by inhibiting the biological function of the Myostatin protein by injecting Myostatin(TM) Blocker into chicken eggs.

Related to Mexican Regulatory Approval

  • Regulatory Approval means any approval or clearance by any governmental agency or agencies having authority to regulate the use or sale of any Licensed Product(s) in the pertinent jurisdiction or territory.

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

  • Key Regulatory Approvals means those sanctions, rulings, consents, orders, exemptions, permits and other approvals (including the lapse, without objection, of a prescribed time under a statute or regulation that states that a transaction may be implemented if a prescribed time lapses following the giving of notice without an objection being made) of Governmental Entities as set out in Schedule C hereto;

  • 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.

  • Regulatory Approvals means any registrations, licenses, authorizations, permits or approvals issued by any Governmental Authority and applications or submissions related to any of the foregoing.

  • Marketing Approval means all approvals, licenses, registrations or authorizations of the Regulatory Authority in a country, necessary for the manufacture, use, storage, import, marketing and sale of a Product in such country.

  • Requisite Regulatory Approvals has the meaning set forth in Section 7.01(b).

  • Drug Approval Application means an application for Regulatory Approval required before commercial sale or use of a Product as a drug in a regulatory jurisdiction.

  • NDA Approval means the Approval of an NDA by the FDA for a Product in the U.S.

  • MAA Approval means approval of an MAA by the applicable Regulatory Authority for marketing and sale of a Product in the Collaborator Territory, but excluding any Pricing and Reimbursement Approval.

  • FDA Approval means the approval by the FDA of a premarket approval application to market and sell a Product, as evidenced by the publication of such approval by the FDA.

  • foreign regulatory authority means a securities commission, exchange or other securities market regulatory authority in a designated foreign jurisdiction;

  • Required Regulatory Approvals means the Seller Required Regulatory Approvals and the Buyer Required Regulatory Approvals.

  • Foreign Financial Regulatory Authority shall have the meaning given by Section 2(a)(50) of the 0000 Xxx.

  • Approval Application means a BLA, NDA or similar application or submission for a Product filed with a Regulatory Authority in a country or group of countries to obtain marketing approval for a biological or pharmaceutical product in that country or group of countries.

  • Pricing Approval means any approval, agreement, determination, or decision establishing prices that can be charged to consumers for a pharmaceutical or biological product or that will be reimbursed by Governmental Authorities for a pharmaceutical or biological product, in each case, in a country where Governmental Authorities approve or determine pricing for pharmaceutical or biological products for reimbursement or otherwise.

  • Marketing Authorization Application or “MAA” means an application for Regulatory Approval in a country, territory or possession.

  • FDA means the United States Food and Drug Administration and any successor agency thereto.

  • Public Procurement Regulatory Authority (PPRA) means the Government Agency responsible for oversight of public procurement.

  • Product Approval means the approval of a Governmental Authority necessary for the marketing and sale of the Product in a given country or regulatory jurisdiction, which may include the approval of an MAA (but shall not include any Pricing Approvals).

  • CFDA means the Code of Federal Domestic Assistance assigned to a federal grant.

  • CFIUS Approval means that any of the following shall have occurred: (a) the review period under the DPA commencing on the date that a CFIUS Notice is accepted by CFIUS shall have expired and Xxx, on the one hand, and Polaris, on the other hand, shall have received written notice from CFIUS to the effect that such review has been concluded and that either the Contemplated Transactions do not constitute a “covered transaction” under the DPA or there are no unresolved national security concerns, and all action under the DPA is concluded with respect to the Contemplated Transactions, (b) an investigation under the DPA shall have been commenced after such review period and CFIUS shall have determined to conclude all action under the DPA without sending a report to the President of the United States, and Xxx, on the one hand, and Polaris, on the other hand, shall have received written notice from CFIUS that either the Contemplated Transactions do not constitute a “covered transaction” under the DPA or there are no unresolved national security concerns, and all action under the DPA is concluded with respect to the Contemplated Transactions, or (c) CFIUS shall have sent a report to the President of the United States requesting the President’s decision and either (i) the President shall have announced a decision not to take any action to suspend or prohibit the Contemplated Transactions or, (ii) the period under the DPA during which the President may announce his decision to take action to suspend, prohibit or place any limitations on the Contemplated Transactions shall have expired without any such action being threatened, announced or taken.

  • national regulatory authority means the body or bodies charged by a Member State with any of the regulatory tasks assigned in this Directive and the Specific Directives;

  • Marketing Authorization means all approvals from the relevant Regulatory Authority necessary to market and sell a Product in any country (including without limitation, all applicable pricing and governmental reimbursement approvals even if not legally required to sell Product in a country).

  • MFDA means the Mutual Fund Dealers Association of Canada;

  • Insurance Regulatory Authority means, with respect to any Insurance Subsidiary, the insurance department or similar Governmental Authority charged with regulating insurance companies or insurance holding companies, in its jurisdiction of domicile and, to the extent that it has regulatory authority over such Insurance Subsidiary, in each other jurisdiction in which such Insurance Subsidiary conducts business or is licensed to conduct business.