miércoles, 27 de julio de 2016

Recursos de Formación

Recursos de Formación

Eurordis, Rare Diseases Europe

La voz de los Pacientes con
Enfermedades Raras en Europa

Recursos de Formación (Inglés)

Los programas de Eurordis de formación y recursos están diseñados para fortalecer la capacidad de los representantes de pacientes a participar en ensayos clínicos, e implicarse en el desarrollo de medicamentos y procesos reguladores en Europa. La formación da poder a los representantes de los pacientes a defender las enfermedades raras de manera eficaz. Más información sobre las condiciones del uso de módulos de formación.
"Empowering Patients, Inspiring Action"

Summer School

A new format was developed for the Summer School in 2015 that combines training for both expert patients and researchers on medicines development.
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Pre-Summer School Training Module

Overview of the topics that are covered at the Summer School as well as exercises and quizzes to familiarise trainees with some of the key concepts and issues presented
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Medical Research

In this section you will be able to learn more about the medicines discovery process, preclinical testing, clinical trials, and methodology and statistics used in medicines development.
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Learn more about the important role of ethical considerations and ethics committees in medicines research and development.
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Regulatory Framework

In this section, you can learn about regulatory affairs including legal framework, guidelines and Health authorities’ requirements that influence the medicines development process.
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European Medicines Agency (EMA)

This section explains how the EMA protects and promotes public health through its committees and working parties, and how patient representatives can get involved.
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Benefit-Risk Assessment and Pharmacovigilance

This section explains how medicines are evaluated to ensure their benefit outweighs their risk and to limit any untended, harmful effect on the body.
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Market Access

In this section you will learn about pharmacoeconomics and the process by which a company gets a medicinal product to market so that it becomes available for patients.
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This section focuses on practical topics for patient advocates and includes presentations on projects which EURORDIS partners and which promote patient involvement.
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