Responsibility. Licensee may use the Inventory provided by [[AstraZeneca:Organization]] solely for the development of Licensed Products pursuant to this Agreement and shall not make any Inventory available to any Third Party except as expressly permitted herein. As between the Parties, Licensee shall have the sole responsibility for, at its expense, Manufacturing (or having Manufactured) and supplying the Licensed Compounds and Licensed Products for its development and commercialization activities in the Territory. [[AstraZeneca:Organization]] shall be under no obligation to Manufacture (or have Manufactured) Licensed Compounds.

Client Responsibility. 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. 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 Client.

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. Client represents, warrants and undertakes to Catalent that:

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. Client represents, warrants and undertakes to Catalent that:

Responsibility. Subject to the terms and conditions of this Agreement, Acadia (and its Affiliates and Sublicensees, as applicable) shall be responsible, at its sole cost and expense, for the Commercialization of all Licensed Products in the Field in the Territory.

Client. Client represents, warrants and covenants to Cardinal Health that:

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.

Responsibility. For each of the [[Unknown Identifier]] and ​ Programs, following the completion of the applicable [[Unknown Identifier]] Technology Transfer or ​ Technology Transfer, # Acadia shall be solely responsible, at its sole expense, for all regulatory activities necessary to obtain and maintain Regulatory Approval of the applicable Licensed Products in the Field in the Territory, and # Acadia will own all Regulatory Materials for such Licensed Products in the Field in the Territory, including all Regulatory Approvals, and will be responsible for the payment of fees and all other associated regulatory costs for such Licensed Products in the Field in the Territory.