Risorse per la formazione (inglese)

I programmi di formazione e le risorse di EURORDIS sono stati sviluppati per rafforzare la capacità dei rapprensentanti dei malati di partecipare alle sperimentazioni cliniche e di essere coinvolti nello sviluppo dei farmaci e nel processo legislativo europeo. La formazione rafforza la capacità dei rappresentanti dei malati di promuovere con efficacia la causa delle malattie rare.

 

Il campo estivo è un’iniziativa avviata da EURORDIS nel 2008. Il campo mira a formare professionalmente i rappresentanti dei malati rari in materia di sperimentazioni cliniche, sviluppo dei farmaci e argomenti riguardanti i regolamenti europei.

EURORDIS Summer School for patient advocates

A group of 40 participants are invited each year to learn about the clinical and regulatory life of medicinal products.

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Clinical research

Aspects of clinical research are covered in this section as well as drug development for small population and the regulatory procedures available for drug licensing.

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Health Technology Assessment

HTA refers to any aspect of health care ranging from prevention programmes to devices, drugs and procedures all aiming to examine the results of healthcare technology use.

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European Medicines Agency

The EMA is a decentralised body of the European Union whose main responsibility is the protection and promotion of public and animal health.

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Summer School Trainers

Each year the Summer School material is taught by experts in the field, find out more about who they are…

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EURORDIS Summer School Alumni

To date more than 110 participants from 27 countries representing more than 45 diseases have been trained.

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Ulteriori informazioni sulle sperimentazioni cliniche con il nuovo corso e-learning sviluppato da EURORDIS

About the course

In 2006, the first capacity-building sessions on clinical trials were held in four countries leading to the EURORDIS Summer School from 2008.

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Module 1 - Methodology

This course explains aspects from study design to choice of endpoints and result analysis.

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Module 2 - Ethics

In this section the e-learning tool can be used to understand the need for ethics is described as well as informed consent and ethics committees.

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Module 3 - Statistics

The module on Statistics complements the current e-learning tool developed to improve patient’s understanding of the drug development process.

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