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  • Search Results for 'Capturing And Reporting Adverse Events In Clinical Research'

Capturing and Reporting Adverse Events in Clinical Research
Capturing and Reporting Adverse Events in Clinical Research
pamella-moone
Safety of the Subject Cena Jones-Bitterman, MPP, CIP, CCRP
Safety of the Subject Cena Jones-Bitterman, MPP, CIP, CCRP
natalia-silvester
SAFETY PRACTICES AND REPORTING IN CLINICAL RESEARCH
SAFETY PRACTICES AND REPORTING IN CLINICAL RESEARCH
min-jolicoeur
Lessons to learn from the reporting of adverse events in RCTs published in four high impact
Lessons to learn from the reporting of adverse events in RCTs published in four high impact
phoebe-click
Dartmouth Human Research Protection Program (HRPP)
Dartmouth Human Research Protection Program (HRPP)
stefany-barnette
Dartmouth Human Research Protection Program (HRPP)
Dartmouth Human Research Protection Program (HRPP)
karlyn-bohler
Adverse Events
Adverse Events
sherrill-nordquist
Did that just happen? And
Did that just happen? And
mitsue-stanley
Adverse Events, Unanticipated Problems, Protocol Deviations
Adverse Events, Unanticipated Problems, Protocol Deviations
faustina-dinatale
FDA Final Rule & Revised NCI Guidelines for Expedited Reporting of Adverse Events
FDA Final Rule & Revised NCI Guidelines for Expedited Reporting of Adverse Events
mitsue-stanley
FDA Final Rule & Revised NCI Guidelines for Expedited Reporting of Adverse Events
FDA Final Rule & Revised NCI Guidelines for Expedited Reporting of Adverse Events
lois-ondreau
Critical Thinking about Institutional Disclosure
Critical Thinking about Institutional Disclosure
trish-goza
Unanticipated Problems
Unanticipated Problems
briana-ranney
Unanticipated Problems
Unanticipated Problems
pamella-moone
Clinical and Institutional Disclosure of Adverse Events to
Clinical and Institutional Disclosure of Adverse Events to
pasty-toler
Expedited Adverse Event
Expedited Adverse Event
pasty-toler
Clinical and Institutional Disclosure of Adverse Events to Patients
Clinical and Institutional Disclosure of Adverse Events to Patients
danika-pritchard
Remote Monitoring of Adverse Events
Remote Monitoring of Adverse Events
conchita-marotz
Office of Research Oversight Reporting: Who, What, When, and Why
Office of Research Oversight Reporting: Who, What, When, and Why
tatiana-dople
Expedited
Expedited
phoebe-click
A Proof-of-Concept Evaluation of Adverse Drug Reaction Surv
A Proof-of-Concept Evaluation of Adverse Drug Reaction Surv
lindy-dunigan
A series of randomised controlled N-of 1 trials in patients
A series of randomised controlled N-of 1 trials in patients
tatyana-admore
A series of randomised controlled N-of 1 trials in patients who have discontinued or are
A series of randomised controlled N-of 1 trials in patients who have discontinued or are
min-jolicoeur
Postmarket monitoring Overview
Postmarket monitoring Overview
conchita-marotz