Clinical Trial Materials. Upon Closing, Seller shall sell, transfer, assign, convey and deliver, or shall cause to be sold, transferred, assigned, conveyed and delivered to Buyer, all of Seller’s rights, title and interest in and to the Clinical Trial Materials.
Clinical Trial Materials. The Company shall provide to PNU clinical ------------------------ trial materials in accordance with the specifications of PNU, and will be invoiced at the Company's fully burdened costs.
Clinical Trial Materials. (i) Vitamin D & Calcium, (ii) Tote Bags/Ice Packs (Sponsor will be responsible for these in all jurisdictions) and (iii) Study Drug Reconciliation — Patient, Site, & Study. Clinical Trial Conduct
Clinical Trial Materials. The inventories of Product (in bulk or finished form as the case may be) and intermediates and supporting documentation, all as identified below: 0xx, 0xx, 16mg and 32mg, placebo and rescue medication tablets stored at [*] (the “Clinical Trial Materials”). Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Company’s application requesting confidential treatment under Rule 406 promulgated under the Securities Act of 1933, as amended; [*] denotes omissions.
Clinical Trial Materials. All Clinical Trial Materials owned by Exxxxxx or its Affiliates as of the Closing Date.
Clinical Trial Materials. Exxxxxx and Sangamo shall mutually agree to the schedule for delivery of the Clinical Trial Materials to Sangamo or its designee.
Clinical Trial Materials. To the Knowledge of Exxxxxx, Schedule 8.4 is a list of all Clinical Trial Materials in existence as of the Signing Date. To the Knowledge of Exxxxxx, all such Clinical Trial Materials were manufactured and stored in compliance with Good Manufacturing Practices and comply with the specifications for such Product. For the purposes of this Section 8.4, “Good Manufacturing Practices” means current good manufacturing practices pursuant to the U.S. Federal Food, Drug and Cosmetics Act as amended (21 USC 301 et seq.) and the relevant U.S. regulations in Title 21 of the U.S. Code of Federal Regulations (including Parts 11, 210, 211, 600 and 611).
Clinical Trial Materials. All drug substance (and active pharmaceutical ingredients used therein) administered in human clinical trials by or on behalf of Company with respect to the Licensed Products or Compounds and the Inventory (a) was manufactured in accordance with the applicable specifications and in compliance with the then-applicable good manufacturing practices and applicable Law, (b) was received, stored, handled and processed in accordance with the applicable specifications therefor, (c) met such specifications at the time of use or, with respect to the Inventory, will meet such specifications upon delivery to Pfizer, and (d) with respect to the Inventory and drug substance containing Compound contracted to be delivered to Company from a Third Party, is free and clear of encumbrances; and
Clinical Trial Materials. Micromet will be responsible for purchasing any additional Clinical Trial Materials from BI pursuant to the BI Process Development Agreement that are required to conduct the Ongoing Clinical Trials and the Combination Study. Serono will be responsible for manufacturing or purchasing all Clinical Trial Materials required to conduct the Serono Program. The costs of manufacturing or purchasing Clinical Trial Materials for the conduct of the Serono Program will be Development Expenses.
Clinical Trial Materials. 5.2.5 In the event that such assistance is necessary, Pharm-Olam will use all reasonable efforts to advise and inform ADVENTRX of needed assistance with sufficient time such that ADVENTRX can provide the requested assistance in a timely manner, understanding the particular importance of any matters raised as Serious Adverse Events as noted in Schedule 1.
