Rights of Data Subjects Participating in the Study. Institution and Pfizer agree that, as between them, Institution is best able to manage requests from Study Subjects for access, amendment, Transfer, restriction, or deletion of Personal Data. In the event that Pfizer and/or CRO receive a request from a Study Subject for such access, amendment, Transfer, restriction, or deletion, Pfizer or CRO will forward the request to Institution. Institution will 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. Institution 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 3 contracts
Samples: Clinical Study Agreement, Clinical Study Agreement, Clinical Study Agreement
Rights of Data Subjects Participating in the Study. Institution and Pfizer agree that, as between them, Institution is best able to manage requests from Study Subjects for access, amendment, Transfer, restriction, or deletion of Personal Data. In the event that Pfizer and/or CRO receive a request from a Study Subject for such access, amendment, Transfer, restriction, or deletion, Pfizer or CRO will forward the request to Institution. Institution will 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. Institution 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. strana, a nie ako právne či regulačné odporúčanie, inštitúcii, či sa podľa Príslušného zákona vyžaduje oznámenie príslušnej vláde.
Appears in 1 contract
Samples: Clinical Study Agreement
Rights of Data Subjects Participating in the Study. Institution and Pfizer agree that, as between them, Institution is best able to manage requests from Study Subjects for access, amendment, Transfer, restriction, or deletion of Personal Data. In the event that Pfizer and/or CRO receive a request from a Study Subject for such access, amendment, Transfer, restriction, or deletion, Pfizer or CRO will may forward the request to Institution. Institution will 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. Institution 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
Rights of Data Subjects Participating in the Study. Institution The Parties and Pfizer agree that, as between them, Institution is best able to manage requests from Study Subjects subjects for access, amendment, Transfer, restriction, or deletion of Personal Data. In the event that Pfizer and/or or CRO receive receives a request from a Study Subject subject for such access, amendment, Transfer, restriction, or deletion, Pfizer or CRO will shall forward the request to Institution. Institution will shall respond to Study Subjectssubjects’ requests for access, amendment, Transfer, restriction, or deletion of Personal Data in accordance with Applicable Law, the Agreement, and any other instructions provided by PfizerPfizer or CRO. Institution 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 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