CALENDAR

EUROCOORD COURSES
& TRAINING ACTIVITIES


23-25 October 2013
Tr@inforPedHIV residential course, Rome, Italy.
More details here

24-25 October 2013
Phylogenetic Workshop for (ultra) Beginners
Malmo, Sweden
More details here

27-29 March 2014
18th International Workshop on HIV Observational Databases (IWHOD), Sitges, Spain. (website)


OTHER TRAINING ACTIVITIES

1-3 September 2013
Antiretroviral Therapy and Comprehensive Care for people living with HIV/AIDS, south of France. More details on the EACS website.

5-7 September 2013
ECReCo - European Clinical Research Course on methodology at large, south of France. More details on the EACS website.

16-19 October 2013
EACS Conference, Brussels, comprehensive research presentations and educational programme.
Abstract deadline 15th July 2013, Late Breaker abstract submission deadline August 28, 2013
For more information check the Conference website.

20-25 January 2014
Swiss Epidemiology Winter School in Wengen, Switzerland. Click here for further details.

Home > Training Modules

TRAINING MODULES

Courses

These e-learning modules have been created as part of the EuroCoord Training and Outreach work package (WP2) as a way to improve research skills to allow researchers to undertake observational research of the highest calibre, and to provide basic and updated laboratory and clinical training to aid the management of HIV-infected patients.

HICDEP   



HIV Cohorts Data Exchange Protocol (HICDEP) is a protocol that allows for the simple sharing of data from HIV cohorts by providing a standard format for datasets.

This module explains more about HICDEP, how it can help you and how you can influence itís development.


Please take a few moments after the course to give us your feedback.

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CoDe       



The coding causes of death in HIV (CoDe) is a uniform coding system for causes of death in HIV-positive persons.

This module explains more about CoDe, what it is, how to access the CoDe protocol and how to apply the CoDe methodology to your study.



Please take a few moments after the course to give us your feedback.

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GCP         



Good Clinical Practice (GCP) is a standard for the design, conduct, performance, monitoring, auditing, recording, analyses, and reporting of clinical trials.

The "Practical Approach to GCP" E-Learning course has been developed to help researchers initiate and conduct randomised clinical trials.

Please take a few moments after the course to give us your feedback.

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Manuscript writing



This module explains how to go about writing a scientific manuscript.





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Cohort studies



This module explains all about Cohort studies.





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Improving Data Quality



This module explains all about improving data quality.





Please take a few moments after the course to give us your feedback.

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