Permits, Registrations and Licenses. 9.1.1 Seres will be responsible, [***], for obtaining, maintaining, updating and remaining in compliance with all permits, licenses and other authorizations during the Term of this Agreement, which are necessary or required under federal, state, and local laws, rules and regulations which are applicable to the use of Product Manufactured by GenIbet hereunder. GenIbet will be responsible for, [***], obtaining and maintaining all generally required permits, registrations and licenses applicable to the Facility and to the production of pharmaceutical and biological products generally to the extent required for GenIbet to carry out its regulatory and Manufacturing obligations hereunder.
9.1.2 Without limitation on the foregoing in Section 9.1.1, GenIbet will prepare and deliver to Seres a Site Master File (SMF) in accordance with the Quality Agreement. Seres may utilize the SMF only in connection with the preparation of regulatory filings related to the Products. Any other use of the SMF by Seres shall require the prior written approval of GenIbet.
Permits, Registrations and Licenses. Prior to commencing removal or relocation, Xxxxx agrees to acquire all necessary permits, registrations, and licenses required for the removal and relocation of the Structure(s) from the County Park. Buyer shall contact the appropriate utility providers, if any, to obtain any necessary permits for the disconnection of utilities. Buyer shall comply with all applicable codes, policies, and regulatory requirements for removal and relocation of the Structure(s). Should removal and relocation require disconnection of utilities, Buyer shall undertake those disconnections in a safe and reasonable manner.
Permits, Registrations and Licenses. (a) NESA will be responsible [***] for obtaining, maintaining, and updating all permits, licenses and other authorizations during the Term, which are necessary or required under Applicable Laws which are applicable to the Commercialization of Product. Seres shall use Commercially Reasonable Efforts to cause its third party suppliers to provide reasonable cooperation and assistance in connection with NESA filing the applicable permits, licenses and other authorizations.
(b) Seres will be responsible [***] in obtaining and maintaining (or instructing its third party suppliers to obtain or maintain, as the case may be) all generally required permits, registrations and licenses applicable to a Manufacturing facility, including any such permits, registrations and licences necessary for the occupancy, access and use of a Manufacturing facility (other than the permits, licenses and authorizations that NESA is | obligated to obtain under Section 6.1(a)), including the production of pharmaceutical and biological products generally to the extent required for Seres to carry out its regulatory and Manufacturing obligations hereunder.
Permits, Registrations and Licenses. (a) Seres will be responsible, at its expense, for obtaining, maintaining, updating and remaining in compliance with all permits, licenses and other authorizations during the Term, which are necessary or required under Applicable Laws and which are applicable to [***] Certain information in this document has been excluded pursuant to Regulation S-K, Item (601)(b)(10). Such excluded information is both (i) not material and (ii) the type that the Registrant treats as private or confidential. the use and commercial distribution of Product Manufactured by Bacthera hereunder. Bacthera will provide reasonable cooperation and assistance in connection with Seres filing the applicable Marketing Approvals at the rates set forth in Section 2.5 of Exhibit 4.
(b) Bacthera will be responsible for, at its expense, obtaining and maintaining all generally required permits, registrations and licenses applicable to the Facility, including any such permits, registrations and licences applicable to the XxX and necessary for the occupancy, access and use of the Facility (other than the permits, licenses and authorizations that Seres is obligated to obtain under Section 12.1(a)), including any that are required for the performance of the Design and Construction Work and to the production of pharmaceutical and biological products generally to the extent required for Bacthera to carry out its regulatory and Manufacturing obligations hereunder.
(c) Additional requirements for permits, licenses and other authorizations relating to the design and construction of the Facility, any other relevant areas for Manufacturing of the Products and any other common areas inside the XxX are set forth in Exhibit 1.
