Բաց թողնել հիմնական բովանդակությունը
TRREE
TRAINING AND RESOURCES IN
RESEARCH
ETHICS EVALUATION
☰
ընդլայնել
Username
Password
Forgotten your username or password?
Դուք մուտք չեք գործել համակարգ։ (
Մուտք
)
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
Հայերեն (hy)
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)
Հետ
Audit
Audit / vérification -- Audit
A systematic and independent examination of trial related activities and documents to determine whether the evaluated trial related activities were conducted, and the data were recorded, analyzed and accurately reported according to the
protocol
,
sponsor
's
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. 1.6
»
Glossary