health-related biomedical or behavioral outcomes. (which may include placebo or other control) to evaluate the effects of those interventions on health-related biomedical or behavioral outcomes. Examples include: drugs/small molecules/compounds biologics devices procedures (e.g., surgical techniques) delivery systems (e.g., telemedicine, face-to-face interviews) strategies to change health-related behavior (e.g., diet, cognitive therapy, exercise, development of new habits) treatment strategies prevention strategies and, diagnostic strategies. to one or more interventions interventions An "intervention" is defined as a manipulation of the subject or subject’s environment for the purpose of modifying one or more health-related biomedical or behavioral processes and/or endpoints. Responsible Conduct of Research (RCR) - HHS ORI ResourcesĪ research study in which one or more human subjects are prospectively assigned prospectively assigned The term "prospectively assigned" refers to a pre-defined process (e.g., randomization) specified in an approved protocol that stipulates the assignment of research subjects (individually or in clusters) to one or more arms (e.g., intervention, placebo, or other control) of a clinical trial.PHS Administrative Action Bulletin Board.What should you do if you Suspect Research Misconduct?.What Happens if there is a Finding of Research Misconduct?.NIH Process for Handling Research Misconduct Allegations.Requirements for Making a Finding of Research Misconduct.Resources to Evaluate Workplace Climate.NIH Expectations, Policies, and Requirements.Supporting a Safe and Respectful Workplace.Resources for Preparing Your Application.Guidance: Rigor and Reproducibility in Grant Applications.Principles and Guidelines for Publishing Preclinical Research.Glossary: Professional Codes, Norms, Ethics Training.Integrity and Confidentiality in NIH Peer Review.Promoting Research Integrity - NIH Initiatives.What can be done to Promote Research Integrity?.Consolidated List of Reviewer Documents.Recommendations for Improving NRSA Fellowship Review.Simplifying Review of Research Project Grant Applications.Applicant/Recipient COVID-19 Update History.Coronavirus Disease 2019 (COVID-19): Information for NIH.Lobbying Guidance for Recipient Activities.Process for Handling Allegations Related to Foreign.Format Pages, Instructions, and Samples.Requirements for Disclosure of Other Support, Foreign Components.Related Notices, Laws, Statements and Reports Communicating and Acknowledging Federal Funding.Human Subjects and Clinical Trial Information Form.Clinical Trial-Specific Review Criteria.Clinical Trial-Specific Funding Opportunities.Basic Experimental Studies Involving Humans (BESH).When Are Alternatives to Animals Used in Research?.How NIH Ensures the Care of Research Animals.Why Properly Designed Experiments Are Critical for Animal.How Animals Have Helped Improve Public Health.
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