All Necessary Approvals Clause Samples
The "All Necessary Approvals" clause requires that all permissions, consents, or authorizations needed from relevant parties or authorities are obtained before certain actions under the agreement can proceed. In practice, this means that a party must secure approvals from regulatory bodies, shareholders, or third parties as applicable before performing obligations such as transferring assets or commencing a project. This clause ensures that the agreement's execution is legally compliant and prevents delays or disputes arising from missing or inadequate permissions.
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All Necessary Approvals. All necessary approvals for the transactions set forth in this Sublease have been obtained, including without limitation, the final approvals of Head Lessor and Owner.
All Necessary Approvals. The Company has obtained all required exemptions, approvals, certifications, registrations and authorizations from all applicable Regulatory Authorities relating to its activities conducted with respect to all Company Pharmaceutical Products as of the date of this Agreement.
All Necessary Approvals. All material certificates, approvals, permits and authorizations of applicable local governmental agencies, and agencies of the State and the federal government have been or will be obtained with respect to the acquisition, construction and installation of the Project and the Project will be acquired, constructed and installed and the Facilities will be operated pursuant to and in accordance with such certificates, approvals, permits and authorizations.
All Necessary Approvals. Such Vendor, and their respective shareholders and board of directors, as the case may be, have taken all necessary or desirable actions to approve or authorize, validly and effectively, the entering into, and the execution, delivery and performance of this agreement and the sale and transfer of the Shares by such Vendor to the Purchaser.
All Necessary Approvals. All material certificates, approvals, permits and authorizations of applicable local governmental agencies, and agencies of the State and the federal government have been or will be obtained with respect to the operation of the Facility, and the Facility will be operated pursuant to and in accordance with such certificates, approvals, permits and authorizations.
All Necessary Approvals. Except as set forth in Section 3.26 of the Disclosure Schedule, Impella has obtained or, prior to the Closing, will obtain (unless such condition is waived by ABIOMED prior to the Closing) all necessary approvals, certifications, registrations and authorizations from, has made or will make all necessary and appropriate applications and other submissions to, and has prepared and maintained or will prepare and maintain all records, studies and other documentation needed to satisfy and demonstrate compliance with the requirements of all applicable Governmental Authorities for its current and past business activities and for the sale of any Product within the European Union and the United States, including any necessary CE Marking certifications, 510(k)s, PMAs, IDEs, Consents from Ethics Committees, line extension letters relating any Product to existing 510(k)s, studies of safety and efficacy, design and engineering specifications and modifications, device history records, certificates of export, and MDRs.
All Necessary Approvals. Except as set forth in Schedule 3.1(r), the Company has obtained or, prior to the Initial Closing, will obtain (unless such condition is waived by the Investor prior to the Initial Closing) all necessary approvals, certifications, registrations and authorizations from, has made or will make all necessary and appropriate applications and other submissions to, and has prepared and maintained or will prepare and maintain all records, studies and other documentation needed to satisfy and demonstrate compliance with the requirements of all applicable Governmental Authorities for its current and past business activities and for the sale of any Product within the European Union and the United States, including any necessary CE Marking certifications, 510(k)s, FDA pre-market approvals (“PMAs”), investigational device exemptions (“IDEs”), Consents from Ethics Committees, line extension letters relating any Product to existing 510(k)s, studies of safety and efficacy, design and engineering specifications and modifications, device history records, certificates of export, and MDRs.
All Necessary Approvals. The Purchaser and its shareholders and board of directors, as the case may be, have taken all necessary or desirable actions to approve or authorize,