Products and Required Permits Sample Clauses

Products and Required Permits. (a) Without limiting the generality of Section 7.08, in connection with the development, testing, manufacture, marketing or sale of each and any Product by the Borrower or any Subsidiary, the Borrower or such Subsidiary shall comply in all material respects with all Required Permits at all times issued by any Government Authority, specifically including the FDA, with respect to such development, testing, manufacture, marketing or sales of such Product by the Borrower or such Subsidiary.
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Products and Required Permits. Without limiting the generality of Section 7.08, in connection with the development, testing, manufacture, marketing or sale of each and any Material Product by Parent or any Subsidiary, Parent or such Subsidiary shall comply in all material respects with all Required Permits, except where such non-compliance could not reasonably be expected to result in (i) the revocation of termination of such Required Permit or (ii) a Material Adverse Effect.
Products and Required Permits. All Products and all Required Permits are listed in the Perfection Certificate (as updated from time to time in accordance with this Agreement).
Products and Required Permits. 1. PRODUCTS
Products and Required Permits. (a) Without limiting the generality of Section 7.08, in connection with the development, testing, manufacture, marketing or sale of each Product by any Loan Party or any Subsidiary, such Loan Party or such Subsidiary shall comply in all material respects with all Required Permits at all times issued by any Governmental Authority, specifically including the FDA and Health Canada, with respect to such development, testing, manufacture, marketing or sales of such Product by such Loan Party or such Subsidiary, except where the failure to do so could not reasonably be expected, either individually or in the aggregate, to have a Material Adverse Effect.
Products and Required Permits. Products: [Please see attached] Required Permits: # Division Current Bacterin Licenses Number Location 1 Devices FDA Registration – CDRH 3008190422 664 Cruiser 2 Devices ISO 13485:2003 Registration FM 557704 664 Cruiser 3 Biologics FDA Registration – CBER and CDRH 3005168462 600 Cruiser 4 Biologics AATB Accreditation 00157 600 Cruiser 5 Biologics California Tissue Bank CNC80509 600 Cruiser 6 Biologics Florida Tissue Bank 126 600 Cruiser 7 Biologics Louisiana License 6383 600 Cruiser 8 Biologics Maryland Tissue Bank TB1366 600 Cruiser 9 Biologics New York Tissue Bank CP135TP110 600 Cruiser 10 Biologics CLIA ID 27D136610 600 Cruiser SCHEDULE 6.13
Products and Required Permits. (a) All Products and all Required Permits applicable to Borrower as of the Effective Date are listed on Schedule 5.10, and Borrower has delivered or made available to Agent a copy of all Required Permits in effect as of the Effective Date;
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Products and Required Permits. The following list includes all Products: KB001A KB003 KB004 The following list includes all material Required Permits: Environmental Health of San Mateo County, Permit No. 12-1657, issued on August 1, 2012 and expires August 1, 2017. Environmental Health of San Mateo County, Permit No. 11-2704, issued on December 14, 2011 and expires December 31, 2013. City of San Francisco, Business License, Business License No. 103547, for period from January 1, 2012 to December 31, 2012. SCHEDULE 6.12
Products and Required Permits. Without limiting the generality of Section 7.08, in connection with the development, testing, manufacture, marketing or sale of each and any Material Product by Parent or any Subsidiary, Parent or such Subsidiary shall comply in all material respects with all Required Permits, except where such non-compliance could not reasonably be expected to result in (i) the revocation of termination of such Required Permit or (ii) a Material Adverse Effect. \DC - 031561/000013 - 10875187 v5 \DC - 031561/000013 - 10875187 v7 \DC - 031561/000013 - 10875187 v9
Products and Required Permits. Without limiting the generality of Section 7.08, in connection with the development, testing, manufacture, marketing or sale of each and any Material Product by Parent or any Subsidiary, Parent or such Subsidiary shall comply in all material respects with all Required Permits, except where such non-compliance could not reasonably be expected to result in (i) the revocation of termination of such Required Permit or (ii) a Material Adverse Effect. 74 \DC - 031561/000013 - 10875187 v5 \DC - 031561/000013 - 10875187 v7 \DC - 031561/000013 - 10875187 v9 7.18 Consent of Licensors. Promptly (but in any event no later than the next Reporting Date) after entering into or becoming bound by any license or agreement (other than over-the-counter software that is commercially available to the public) after the date hereof, the failure, breach or termination of which could reasonably be expected to have a Material Adverse Effect, the Note Parties shall (a) provide written notice to the Purchasers of the material terms of such license or agreement, all of which shall constitute “Information” pursuant to Section 12.07, regardless of whether marked confidential, and (b) in good faith take such commercially reasonable actions as the Collateral Agent or Required Purchasers may reasonably request to obtain the consent of, or waiver by, any Person whose consent or waiver is necessary for (i) the applicable Note Party’s interest in such licenses or contract rights to be deemed Collateral and for the Collateral Agent to have a security interest in it that might otherwise be restricted by the terms of the applicable license or agreement, whether now existing or entered into in the future and (ii) the Collateral Agent to have the ability in the event of a liquidation of any of the Collateral to dispose of such Collateral in accordance with the Collateral Agent’s rights and remedies under this Agreement and the other Note Documents, subject to such Collateral remaining subject to such license or other agreement notwithstanding such disposal; provided, that, the failure to obtain any such consent or waiver shall not by itself constitute a Default. 7.19
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