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Radio pharmaceutical Therapy Dose Documentation Form Y90 () A. WRITTEN DIRECTIVE: 1. Pt Name: 3. Female or Male 2. MR#: 4. Radio pharmaceutical (Including Isotope): Y90 () 6. Date of Administration:
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Protocol and dose formopen is a document that outlines the details of a clinical trial, including the study protocol and dosing information for participants.
The sponsor or sponsor-investigator is required to file the protocol and dose formopen for a clinical trial.
The protocol and dose formopen can be filled out by providing all the required information, including study objectives, study design, dosing regimen, and other relevant details.
The purpose of protocol and dose formopen is to ensure that all necessary information about a clinical trial is documented and communicated to relevant parties.
The protocol and dose formopen must include details such as study objectives, study design, dosing regimen, inclusion and exclusion criteria, and safety monitoring plan.
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