SnET2 for Ophthalmology Sample Clauses

SnET2 for Ophthalmology. Notwithstanding anything herein to the contrary, for Ophthalmology, unless otherwise determined by the Ophthalmology Operating Committee, PDTI shall be responsible for conducting all necessary Preclinical Tests and Phase I and Phase II Clinical Tests for SnET2 to be used in any Ophthalmology indications within the Fields. The Out-of-Pocket Expenses associated with Preclinical Tests, Phase I and Phase II Clinical Tests being conducted by PDT on the Ophthalmology Effective Date, or conducted by PDT thereafter, shall be refunded by Pharmacia, provided that these studies have been conducted in agreement with the Ophthalmology Operating Committee. Pharmacia shall be responsible for conducting and shall bear all costs associated with Phase III Clinical Tests of SnET2 to be used in all Ophthalmology indications, as well as for all post-NDA approval studies which may be necessary; provided, however, that the Ophthalmology Operating Committee has the right to determine, in its reasonable judgment, whether to proceed to Phase III Clinical Tests as to any Ophthalmology indication. PDTI shall supply to Pharmacia SnET2 and Light Devices to enable Pharmacia to carry out Phase III Clinical Tests required to support an NDA for SnET2. The actual costs of SnET2 and Light Devices for all Clinical Test phases shall be shared equally by the parties hereto."
Sample 1
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SnET2 for Ophthalmology. Unless otherwise determined by the parties, Miravant shall be responsible for conducting all necessary Preclinical Tests and Phase I and Phase II Clinical Tests for SnET2 to be used in any indications in the Field. The Out-of-Pocket Expenses associated with Preclinical Tests, Phase I and Phase II Clinical Tests being conducted by Miravant on the Effective Date, or conducted by Miravant thereafter, shall be reimbursed by P&U AB; provided, that these studies were conducted in accordance with the protocols and budget approved by the Operating Committee. Miravant shall be responsible for conducting Phase III Clinical Tests of SnET2 in the United States, and P&U AB shall reimburse Miravant for all Out of Pocket Expenses so incurred; provided, that these studies were conducted in accordance with the protocols and budgets approved by the Operating Committee. P&U AB will be responsible for conducting Phase III Clinical Tests of SnET2 in the rest of the world. P&U AB shall be responsible for conducting all post-NDA approval studies which may be necessary. The Operating Committee has the right to determine, in its reasonable judgment, whether to proceed to Phase III Clinical Tests for any indication in the Field. All Clinical Tests shall be conducted in accordance with the protocols approved by the Operating Committee. Miravant shall supply to P&U AB SnET2 and Light Devices to enable P&U AB to carry out such Phase III Clinical Tests conducted by it. The actual costs of SnET2 and Light Devices for all Clinical Test phases shall be shared equally by the parties hereto.
Sample 1

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