Skip to main content
TRREE
TRAINING AND RESOURCES IN
RESEARCH
ETHICS EVALUATION
☰
Expand
Username
Password
Forgotten your username or password?
You are not logged in. (
Log in
)
TRREE
E-Learning Modules
1 Introduction to Research Ethics
2 Research Ethics Evaluation
3 Informed Consent
4 Good Clinical Practice (GCP)
5.1 HIV Vaccine Trials
5.2 Adolescent involvement in HIV prevention trials
5.3 Public Health Research Ethics
Regulatory Frameworks
AFRICA
⚑ Burkina Faso
⚑ Cameroon
⚑ Côte d'Ivoire
⚑ Kenya
⚑ Mali
⚑ Niger
⚑ Nigeria
⚑ Senegal
⚑ South Africa
AMERICAS
⚑ Argentina
EUROPE
⚑ Armenia
⚑ Finland
⚑ France
⚑ Germany
⚑ Lithuania
⚑ Poland
⚑ Portugal
⚑ Switzerland
Resources
Glossary
Bibliography
Publications about TRREE
About
About TRREE
Team
Contact Us
English (en)
Deutsch (de)
English (en)
Español - Argentina (es_ar)
Español - Internacional (es)
Français (fr)
Kiswahili (sw)
Latviešu (lv)
Lietuvių (lt)
Polski (pl)
Português - Brasil (pt_br)
Português - Portugal (pt)
Română (ro)
Suomi (fi)
Հայերեն (hy)
正體中文 (zh_tw)
Back
Monitoring
Surveillance /
monitor
ing -- Monitoring
The act of overseeing the progress of a clinical trial, and of ensuring that it is conducted, recorded, and reported in accordance with the
protocol
,
Standard Operating Procedures (SOPs)
,
Good Clinical Practice (GCP)
, and the
applicable regulatory requirement(s)
.
International Conference on Harmonisation (ICH) – Guideline for Good Clinical Practice (GCP) E6 (R1), Glossary art. 1.38
»
Glossary