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Precision×Medicine×Study×GroupPRAEGNANT×Studied×and×Biomaterial×Proposal×FormNoQuestion123Proposal×Identifier (to×be completed×by PREGNANT×group)TitleContact×Information(Name, ×Institution,
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Praegnant studie data refers to clinical trial data related to pregnant individuals.
The sponsor or entity responsible for conducting the clinical trial is required to file praegnant studie data.
Praegnant studie data can be filled out electronically on the designated platform provided by the regulatory authorities.
The purpose of praegnant studie data is to ensure the safety and efficacy of medical treatments for pregnant individuals.
Praegnant studie data must include information on the study design, participant demographics, adverse events, and pregnancy outcomes.
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