Common use of Definition Trial Drug Clause in Contracts

Definition Trial Drug. In addition to the Investigational Product, Sponsor may provide or arrange for provision of other drug products, if applicable, to be used in the Trial in accordance with the Protocol. The Investigational Product and such other drug products are collectively referred to herein as “Trial Drug”. zpracováváním osobních údajů Subjektu hodnocení v souvislosti s Klinickým hodnocením, v souladu s formulářem IS poskytnutým Zadavatelem a schváleným příslušnou IRB/EC,

Appears in 1 contract

Samples: Clinical Trial Agreement

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Definition Trial Drug. In addition to the Investigational Product, Sponsor may will provide or arrange for provision of other drug products, if applicable, to be used in the Trial in accordance with the Protocol. The Investigational Product and such other drug products are collectively referred to herein as “Trial Drug”. zpracováváním osobních údajů Subjektu hodnocení v souvislosti s Klinickým hodnocením, v souladu s formulářem IS poskytnutým Zadavatelem a schváleným příslušnou IRB/EC,.

Appears in 1 contract

Samples: Clinical Trial Agreement

Definition Trial Drug. In addition to the Investigational Product, Sponsor may provide or arrange for provision of other drug products, if applicable, to be used in the Trial in accordance with the Protocol. The Investigational Product and such other drug products are collectively referred to herein as “Trial Drug”. zpracováváním osobních údajů Subjektu hodnocení v souvislosti s Klinickým hodnocením, v souladu s formulářem IS poskytnutým Zadavatelem a schváleným příslušnou IRB/EC,1.7.2

Appears in 1 contract

Samples: Clinical Trial Agreement

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Definition Trial Drug. In addition to the Investigational Product, Sponsor may provide or arrange for provision of other drug products, if applicable, to be used in the Trial in accordance with the Protocol. The Investigational Product and such other drug products are collectively referred to herein as “Trial Drug”. zpracováváním osobních údajů Subjektu hodnocení v souvislosti s Klinickým hodnocením, v souladu s formulářem IS poskytnutým Zadavatelem a schváleným příslušnou IRB/EC,.

Appears in 1 contract

Samples: Clinical Trial Agreement

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