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This document outlines the process for researchers to obtain Maryland PRAMS data from the Department of Health and Mental Hygiene. It details the necessary approvals required from the Principal Investigator
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The prams_irb_packet is a packet of forms and documents used by the Maryland Department of Health to collect data related to the Pregnancy Risk Assessment Monitoring System (PRAMS) and Institutional Review Board (IRB) protocols.
Healthcare providers and researchers in Maryland who are conducting studies under the PRAMS and IRB protocols are required to file the prams_irb_packet with the Maryland Department of Health.
To fill out the prams_irb_packet, healthcare providers and researchers need to complete the forms provided in the packet according to the instructions provided. The packet may include demographic information of the study participants, consent forms, questionnaires, and other required documents.
The prams_irb_packet is used to collect data on the health of pregnant women and their infants, and to ensure that studies conducted under the PRAMS and IRB protocols meet ethical and regulatory standards.
The specific information that must be reported on the prams_irb_packet may vary depending on the study, but it may include demographic information of the study participants, medical history, prenatal care information, pregnancy outcomes, and other relevant data.
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