Client Responsibility. For clarity, the parties agree that in reviewing the documents referred to in [subsections (b) and (c)])] above, Patheon’s role will be limited to verifying the accuracy of the description of the work undertaken or to be undertaken by Patheon. Subject to the foregoing, Patheon will not assume any responsibility for the accuracy of any application for receipt of an approval by a Regulatory Authority. The Client is solely responsible for the preparation and filing of the application for approval by the Regulatory Authority and any relevant costs will be borne by the Client, excepts as otherwise provided in this Section 7.8.
Client Responsibility. For clarity, the parties agree that in reviewing the documents referred to in [clause (b) above], [[Organization A:Organization]]'s role will be limited to verifying the accuracy of the description of the work undertaken or to be undertaken by [[Organization A:Organization]]. Subject to the foregoing, [[Organization A:Organization]] will not assume any responsibility for the accuracy of any application for receipt of an approval by a Regulatory Authority. The Client is solely responsible for the preparation and filing of the application for approval by the Regulatory Authority and any relevant costs will be borne by the Client.
Client Responsibility. For clarity, the parties agree that in reviewing the documents referred to in [clause (b) above], Patheon’s role will be limited to verifying the accuracy of the description of the work undertaken or to be undertaken by Patheon. Subject to the foregoing, Patheon will not assume any responsibility for the accuracy of any application for receipt of an approval by a Regulatory Authority. The Client is solely responsible for the preparation and filing of the application for approval by the Regulatory Authority and any relevant costs will be borne by the Client.
Client. Client represents, warrants and undertakes to Catalent that:
Client. Client represents, warrants and covenants to Cardinal Health that:
Responsibility. [[Organization A:Organization]] shall use Commercially Reasonable Efforts to Develop and obtain Regulatory Approvals for at least one Licensed Product in the Field and in the Territory in accordance with the Development Plan.
Responsibility. [[Organization A:Organization]] shall be solely responsible for, at [[Organization A:Organization]]’s cost and expense, preparing, filing and maintaining, and shall own, the Regulatory Approvals, IB, IND and other regulatory filings for the Licensed Product in the Field and in the Territory. [[Organization A:Organization]] shall keep the [[Agenus:Organization]] Manager informed of scheduled meetings, teleconferences and other interactions with regulators relevant to the Licensed Product.
Responsibility. It is understood and agreed that [[Organization A:Organization]] is solely responsible for searching for, identifying, evaluating or obtaining access to, Patent Rights Controlled by Third Parties (expressly excluding the [[Agenus:Organization]] IP) that may be infringed by the Development, Manufacture or Commercialization of the Licensed Product in accordance with this Agreement. [[Agenus:Organization]] shall have no responsibility or liability to [[Organization A:Organization]] with respect to such Third Party Patent Rights. In the event that either Party receives any notice of potential infringement of any Third Party Patent Rights as a result of, or otherwise impacting, the Exploitation of the Licensed Product, it shall promptly notify the other Party.
Responsibility. It is understood and agreed that searching for, identification and evaluation of Third-Party Patents that may apply to any Program Antibodies based on sequence, Target or the like is the responsibility of iTeos, and that [[Adimab:Organization]] shall have no responsibility for the foregoing nor liability if any such Third-Party Patents exist (except as provided in [Section 4.5(b)] above).
Responsibility. It is understood and agreed that Betta is solely responsible for searching for, identifying, evaluating or obtaining access to, Patent Rights Controlled by Third Parties (expressly excluding the Licensed IP) that may be infringed by Betta’s Development, Manufacture or Commercialization of the Licensed Antibodies or Licensed Products in the Field in the Territory in accordance with this Agreement. [[Agenus:Organization]] will have no responsibility or liability to Betta with respect to such Third Party Patent Rights. In the event that either Party receives any notice of potential infringement of any Third Party Patent Rights as a result of, or otherwise impacting, the Exploitation of the Licensed Product, it will promptly notify the other Party.
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