Other Documents and Materials Clause Samples
Other Documents and Materials. Such other assurances, certificates, documents, approvals, consents, materials or opinions as the Administrative Agent or the Required Lenders reasonably may require.
Other Documents and Materials. Such other assurances, certificates, documents, approvals, consents, materials or opinions as the Lender reasonably may require.
Other Documents and Materials. Seller shall provide copies to, or make available for inspection by, Purchaser such non-proprietary, non-privileged, documents and materials relating to the Assets as Purchaser may reasonably request, to the extent the same are in Seller's possession or control or are in the possession or control of Seller’s agents.
Other Documents and Materials. A. Inspection of Files. Upon reasonable request during the Due ------------------- Diligence Period, Seller will make its files, books, and records pertaining to the Property reasonably available for inspection and copying by Buyer in Los Angeles and/or Santa ▇▇▇▇▇▇ (at the election of Seller), to the extent that the same are Known to Seller to be in the possession of any of the Seller Parties, except: (i) appraisals or valuation information, (ii) internal memoranda, communications, analyses, and business plans, (iii) correspondence and other materials to or from legal counsel for Seller or any of the Seller Parties, (iv) correspondence and other materials pertaining to potential other buyers, and (v) other information which is privileged, confidential, or proprietary.
Other Documents and Materials. To the extent not included in the Data Room, Endo shall provide BDSI with copies of all Regulatory Approvals and Regulatory Submissions as soon as possible following the Effective Date. In addition, in each case, pursuant to the Transition Services Agreement and to the extent in Endo’s or its Affiliates’ possession or control, Endo shall provide to BDSI all customer complaints, adverse event reports, other similar records related to the Product, its use, or any pharmacovigilance or similar functions with respect thereto, any records or documentation concerning any clinical study or Manufacture of the Product, and any documentation related to any of the foregoing.