|CCM | IACUC | INVO | IRB | OECC | ORD | ORI | ORIS | ORPFC | ORS | OSR | SIS|
Policy and procedures for handling alleged research misconduct, including allegations of falsification, fabrication, or plagiarism.
Policy providing protection from retaliation for individuals who bring forward concerns in good faith.
Policy describing the basis of data ownership, standards for the collection and retention of data, and requirements for data access.
Instructions and information for the mandatory registration of clinical trials in clinicaltrials.gov.
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