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Clinical Trials

all-covered

CRAs are essential to ensure that studies are conducted efficiently, ethically and in compliance with regulatory standards and Good Clinical Practices. ​

FreeCRA is by our side to:

  • select sites,

  • assess feasibility,

  • monitor trials,

  • deliver site training and support,

  • document your study,

  • oversee patient safety and data integrity. 

Employés de l'hôpital

Discover all our services

START UP SERVICES & FEASIBILITY

Contracts set a secure framework for your trial. Our CRAs can make sure they become a facilitator.

REGULATORY

Compliance can jeopardize your trials. Our CRAs are there to ensure you are in line.

MONITORING

Monitoring a trial activities is crucial to ensuring the success and compliance of the trial.

STUDY NURSING

At each step of the way, it is essential to make sure processes are strictly respected. We take care of that. 

FreeCRA Clinical Research Support

CCI France/Espagne

Passeig de Gràcia, 2

08007 Barcelona, SPAIN

contact@freecra.com

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FreeCRA is a network of Clinical Research Associates (CRAs) operating in Spain and in Europe for more complex project.

Merci pour votre envoi !

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