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DMID160095 ProtocolVersionDate: 3/22/2019 CONSENTFORM TITLEOFRESEARCH:UAB IRB Approved 22May2019 until 21May2020APhaseII,Singletree, SingleArmInvestigationofOralValganciclovir TherapyinInfantswithAsymptomaticCongenitalCytomegalovirus InfectionSCREENINGCONSENT IRBPROTOCOLNO.:IRB300001001INVESTIGATOR:DavidKimberlin,
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The consent form title refers to a legal document that outlines the agreement between parties regarding the handling of personal information or participation in a study or activity.
Individuals or organizations that conduct research, collect data, or require permission for participation in activities involving personal information are required to file the consent form title.
To fill out the consent form title, carefully read the instructions provided, fill in the required fields, provide necessary details about the purpose, risks, and rights, and obtain signatures from all parties involved.
The purpose of the consent form title is to ensure that all participants are informed about the study or activity and voluntarily agree to participate, safeguarding their rights and interests.
The consent form title must report information about the study's purpose, procedures involved, potential risks, benefits, confidentiality measures, and the right to withdraw consent at any time.
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