Common use of Rights of Data Subjects Participating in the Study Clause in Contracts

Rights of Data Subjects Participating in the Study. The Parties and Pfizer agree that, as between them, Institution and Principal Investigator are best able to manage requests from Study subjects for access, amendment, Transfer, restriction, or deletion of Personal Data. In the event that Pfizer or CRO receives a request from a Study subject for such access, amendment, Transfer, restriction, or deletion, Pfizer or CRO shall forward the request to Institution and Principal Investigator. Institution and Principal Investigator shall respond to Study subjects’ requests for access, amendment, Transfer, restriction, or deletion of Personal Data in accordance with Applicable Law, the Agreement, and any other instructions provided by Pfizer or CRO. Institution and Principal Investigator acknowledge that in order to maintain the integrity of Study results, the ability to amend, restrict, or delete Personal Data may be limited, in accordance with Applicable Law. Pfizer acknowledges that Study subjects may withdraw their informed consent to Study participation and their consent to Processing of Personal Data at any time.

Appears in 1 contract

Samples: Clinical Study Agreement

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Rights of Data Subjects Participating in the Study. The Parties and Pfizer agree that, as between them, Institution and Principal Investigator are Health Services Provider is best able to manage requests from Study subjects for access, amendment, Transfer, restriction, or deletion of Personal Data. In the event that Pfizer or CRO receives a request from a Study subject for such access, amendment, Transfer, restriction, or deletion, Pfizer or CRO shall forward the request to Institution and Principal InvestigatorHealth Services Provider. Institution and Principal Investigator Health Services Provider shall respond to Study subjects’ requests for access, amendment, Transfer, restriction, or deletion of Personal Data in accordance with Applicable Law, the Agreement, and any other instructions provided by Pfizer or CRO. Institution and Principal Investigator acknowledge Health Services Provider acknowledges that in order to maintain the integrity of Study results, the ability to amend, restrict, or delete Personal Data may be limited, in accordance with Applicable Law. Pfizer acknowledges that Study subjects may withdraw their informed consent to Study participation and their consent to Processing of Personal Data at any time.

Appears in 1 contract

Samples: Clinical Study Agreement

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