Study Reproductions Sample Clauses

Study Reproductions. Reproductions may be made of all concerts, or from archival reproduction media, for the purpose of being loaned in advance of a performance to be studied by conductors, guest artists, and composers of the works performed in the reproductions, under the following conditions: (1) The Union shall be given at least five (5) business days advance written notification of the making of each such reproduction and shall be entitled to have present a non-performing representative designated by it to observe all aspects of the reproduction process. Upon such prior written notice to the Union, study reproductions made by or at the expense of the Employer may be loaned to conductors, guest artists and composers of the works performed in the reproductions for study purposes only, conditioned on the Employer obtaining an agreement in a form furnished by the Union which provides that such reproductions will not be further reproduced, will be returned after use and will not be used for any purpose not specifically permitted herein. (2) All video study reproductions, at the time made (or, if copied from archival reproductions, at the time copied), shall have the words "Study Reproduction" superimposed upon the entire width of the screen, in letters at least one-tenth (1/10th) of the screen height, for not less than one (1) second in duration not less frequently than once each minute, and all audio reproductions, including the audio part of a video reproduction, shall have a silent period of not less than one-half (½) second in duration not less frequently than once each minute. (3) Study reproductions shall be delivered to the Union for erasing or destruction after they have been returned by the borrower, and if the media is of a reusable type, the Union shall return erased media to the Employer in a timely fashion.
Sample 1
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Related to Study Reproductions

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  • Commercialization Reports Throughout the term of this Agreement and during the Sell-Off Period, and within thirty (30) days of December 31st of each year, Company will deliver to University written reports of Company’s and Sublicensees’ efforts and plans to develop and commercialize the innovations covered by the Licensed Rights and to make and sell Licensed Products. Company will have no obligation to prepare commercialization reports in years where (a) Company delivers to University a written Sales Report with active sales, and (b) Company has fulfilled all Performance Milestones. In relation to each of the Performance Milestones each commercialization report will include sufficient information to demonstrate achievement of those Performance Milestones and will set out timeframes and plans for achieving those Performance Milestones which have not yet been met.

  • Tests and Preclinical and Clinical Trials The preclinical studies and clinical trials conducted by or, to the Company’s knowledge, on behalf of the Company, that are described in the Registration Statement, the Pricing Disclosure Package and the Prospectus, as applicable, and are intended to be submitted to the U.S. Food and Drug Administration (the “FDA”) or other comparable government entities, were and, if still ongoing, are being conducted in all material respects in accordance with experimental protocols, procedures and controls pursuant to accepted professional scientific standards and all Authorizations and Applicable Laws, including, without limitation, current Good Clinical Practices and Good Laboratory Practices and any applicable rules and regulations of the jurisdiction in which such trials and studies are being conducted; the descriptions of the results of such studies and trials contained in the Registration Statement, the Pricing Disclosure Package and the Prospectus are, to the Company’s knowledge, accurate and complete in all material respects and fairly present the data derived from such studies and trials; except to the extent disclosed in the Registration Statement, the Pricing Disclosure Package and the Prospectus, the Company is not aware of any studies or trials, the results of which the Company believes reasonably call into question the study or trial results described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus when viewed in the context in which such results are described and the clinical stage of development; and, except to the extent disclosed in the Registration Statement, the Pricing Disclosure Package or the Prospectus, the Company has not received any written notices or written correspondence from the FDA or any governmental entity requiring the termination or suspension of any preclinical studies or clinical trials conducted by or on behalf of the Company, other than ordinary course communications with respect to modifications in connection with the design and implementation of such trials, copies of which communications have been made available to you.

  • Development Records Each Party shall maintain complete, current and accurate records of all Development activities conducted by it hereunder, and all data and other information resulting from such activities. Such records shall fully and properly reflect all work done and results achieved in the performance of the Development activities in good scientific manner appropriate for regulatory and patent purposes. Each Party shall document all non-clinical studies and Clinical Trials in formal written study reports according to Applicable Laws and national and international guidelines (e.g., ICH, cGCP, cGLP, and cGMP).

  • Protocols Each party hereby agrees that the inclusion of additional protocols may be required to make this Agreement specific. All such protocols shall be negotiated, determined and agreed upon by both parties hereto.

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