Federal Regulations [45 CFR 46.103(b)(5) and 21 CFR 56.108(b)(1)] and UAB IRB policy (POL006) requires Principal Investigators of all human subject’s research (FDA-regulated or not), and their ...
Situations may occur during implementation of a research study, after a participant withdraws or completes their participation, or after study completion that warrant assessment by Research Integrity ...
Overall Count and Share for 'Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, RAS' based on the 12-month time frame mentioned above. Note: Articles may be assigned to ...
Understanding and solving environmental challenges increasingly requires a combination of expertise from across multiple disciplines. This Research Experiences for Undergraduates (REU) program ...
Per federal regulations, University and affiliate researchers must notify the IRB of unanticipated problems that involve risks to participants or others (henceforth referenced as Unanticipated ...
Most Americans have positive overall views of medical doctors and medical research scientists. But they have more mixed assessments when it comes to trust-related judgments, especially for medical ...
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