Common Contracts

4 similar null contracts

Instruction Pages The information set out below provides a checklist of information that needs to be included in the Contract Research Organisation model Clinical Investigation Agreement (CRO-mCIA) in preparation for execution by the Parties. It is...
December 13th, 2023
  • Filed
    December 13th, 2023

Add, remove and / or update recitals as applicable to the Clinical Investigation (as a preamble to the Agreement, such changes do not constitute modification to the template Agreement). Recital E should be completed where a corporate Affiliate of the Sponsor is formally empowered by the Sponsor to sign the Agreement on behalf of the Sponsor thereby binding the Sponsor as Party to the Agreement (and should be removed where this is not the case). Recital F should be retained if the Trial Site is in Northern Ireland and otherwise deleted.

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Instruction Pages The information set out below provides a checklist of information that needs to be included in the Clinical Research Organisation model Clinical Investigation Agreement (CRO-mCIA) in preparation for execution by the Parties. It is...
September 27th, 2023
  • Filed
    September 27th, 2023

Add, remove and / or update recitals as applicable to the Clinical Investigation (as a preamble to the Agreement, such changes do not constitute modification to the template Agreement). Recital E should be completed where a corporate Affiliate of the Sponsor is formally empowered by the Sponsor to sign the Agreement on behalf of the Sponsor thereby binding the Sponsor as Party to the Agreement (and should be removed where this is not the case). Recital F should be retained if the Trial Site is in Northern Ireland and otherwise deleted.

Instruction Pages The information set out below provides a checklist of information that needs to be included in the Clinical Research Organisation model Clinical Investigation Agreement (CRO-mCIA) in preparation for execution by the Parties. It is...
March 23rd, 2023
  • Filed
    March 23rd, 2023

Add, remove and / or update recitals as applicable to the Clinical Investigation (as a preamble to the Agreement, such changes do not constitute modification to the template Agreement). Recital E should be completed where a corporate Affiliate of the Sponsor is formally empowered by the Sponsor to sign the Agreement on behalf of the Sponsor thereby binding the Sponsor as Party to the Agreement (and should be removed where this is not the case). Recital F should be retained if the Trial Site is in Northern Ireland and otherwise deleted.

The information set out below provides a checklist of information that needs to be included in the model Clinical Research Organisation Clinical Investigation Agreement (CRO-mCIA) in preparation for execution by the Parties. It is the responsibility...
England and Wales • September 20th, 2021

Add, remove and/or update recitals as applicable to the Clinical Investigation (as a preamble to the Agreement, such changes do not constitute modification to the template Agreement). Recital E should be completed where a corporate Affiliate of the Sponsor is formally empowered by the Sponsor to sign the Agreement on behalf of the Sponsor thereby binding the Sponsor as Party to the Agreement (and should be removed where this is not the case). Recital F should be retained if the Trial Site is in Northern Ireland and otherwise deleted.

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