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Research participant
Office for Research Procedure
Informed Consent, AI Technologies, and Public Health Emergencies
RESEARCH STANDARD OPERATING PROCEDURES Documentation of Research Study Procedures in the Patients' Health Record
METHODS for REMOTE CLINICAL TRIALS Authors: Jennifer Dahne, Phd and Matthew J
Dear Potential Research Participant, Thank You for Your Interest in This
Doctor-Patient Communication: the Experiences of Black Caribbean Women Patients with Diabetes
The Barriers Encountered in Telemedicine Implementation by Health Care Practitioners
Sample Informed Consent Language Library Describing Technologies Used in Research
Whatsapp in Health Communication: the Case of Eye Health in Deprived Settings in India
Protecting Human Research Participants NIH Office of Extramural Research Introduction
Strategies for Catalyzing Clinicians' Support of Telemedicine Programs
Importance of Consent in the Research Naresh Manandhar1, Sunil Kumar Joshi1 1Department of Community Medicine, Kathmandu Medical College, Sinamangal
Increasing Access to Clinical Research Using an Innovative Mobile Recruitment Approach: the (More) Concept
16-1 Glossary
Clinical Research Core Research Elements Value Case
A Private Right of Action for Informed Consent in Research
The Creation and Validation of the Dynamic Injury Screening Tool for the Lower
Advancing Clinical and Transformational Research with Informatics at the University of Kansas Medical Center
Top View
Assessing Clinical Software User Needs for Improved Clinical Decision Support Tools
Research Participant Registry Collects Must Be Registered
Research Participant Perception Survey (RPPS) Carrie Dykes, Phd SCORE December 16, 2020 Learning Objectives
EXTENDING OCCUPATIONAL THERAPY SERVICES to RURAL MISSISSIPPI Melody M
Towards Patient-Centered Stewardship of Research Data and Research Participant Recruitment with Blockchain Technology
Team-Based Electronic Communication in the Care of Patients with Complex Conditions
Informed Consent to Participate in Research
Placement of a Research Consent Form in the Participant's Medical
Doctor, Nurse, Patient Relationships: Negotiating Roles and Power a Case Study of Decision-Making for C-Sections
LETTER of INFORMATION and CONSENT to PARTICIPATE in a RESEARCH STUDY
Virtual Clinical Trials Challenges and Opportunities: Workshop Highlights
Use of Data from the Electronic Health Record for Health Research – Current Governance Challenges and Potential Approaches
What Results Should Be Returned from Opportunistic Screening in Translational Research?
All Instructions (In RED) and Text Not Applicable to The
The Health Insurance Portability and Accountability Act (HIPAA) Excerpted from the UTC IRB Policy
My Name Is Adam Based on a True Patient S Journey in Research by National Healthcare Group a Biennial Research Report 2008-2009
Reviewing Clinical Trials: a Guide for the Ethics Committee
A Survey of Practices for the Use of Electronic Health Records to Support Research Recruitment