№ files_lp_3_process_7_104870
Consent form outlining permissions for researchers to access and use health data of pregnant partners whose partners are enrolled in a clinical study, including collection of information from doctors and follow-up after birth.
Year: 2026
Region / City: United States
Subject: Medical Research, Pregnancy, Clinical Trials
Document Type: Informed Consent Form
Institution / Organization: Weill Cornell Medicine Institutional Review Board
Principal Investigator: [PI name]
Study Sponsor: [study sponsor]
Target Audience: Pregnant partners of study participants
Study Period: During pregnancy and 30 days post-delivery
Document Version Date: [Version date]
Data Usage: Collection and analysis of health information for research purposes
Confidentiality Measures: Data storage, limited access, de-identification, legal disclosures if required
Price: 8 / 10 USD
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