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Search Results for 'Capturing And Reporting Adverse Events In Clinical Research'
FDA Final Rule & Revised CTEP Guidelines for Expedited
stefany-barnette
Society for Yoga Research
myesha-ticknor
AE/SAE/EAE Identification and Reporting
giovanna-bartolotta
Expedited Reporting Darlene Kitterman,
jane-oiler
Pharmacovigilance 1 Dr. Ganesh Uchit
liane-varnes
Critical Thinking about Institutional Disclosure
alexa-scheidler
Office of Research Oversight
mitsue-stanley
Adverse Effects of Single Dose Gentamicin in Adults
alexa-scheidler
The IND and Clinical Trial Management
kittie-lecroy
Post Balance Sheet Events
stefany-barnette
Symptom Management of Novel Agents
yoshiko-marsland
Terminologies in Clinical Research
trish-goza
Clinical Alerts and ADRs - the importance of reporting
pasty-toler
Clinical Alerts and ADRs - the importance of reporting
lindy-dunigan
Ira S. Goodman
yoshiko-marsland
Managing Sponsorship
tatiana-dople
Event Repository Reporting
calandra-battersby
Reportable Events and Incidents Training
lois-ondreau
“The Death Worm”: A SMART-on-FHIR, Clinical Decision Support Tool for Mortality Reporting
mitsue-stanley
Results of the AAHRPP Visit
luanne-stotts
Results of the AAHRPP Visit
phoebe-click
Good Clinical Practice (GCP) and Monitoring Practices
karlyn-bohler
Adult Male Circumcision Devices
conchita-marotz
Short-Term Use of Oral Corticosteroids and Related Harms Among Adults in the United
alexa-scheidler
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