Our Professional Team is ready to collaborate with you in all the steps of your clinical study in Phase I, Phase II, Phase III and Phase IV. We are prepared to help you from the initial organization of your clinical research plans, the set up study activities, monitoring and follow-up for a successful result.

We offer you the following services in clinical trials:

Clinical Trial Management Services:

Feasibilitiy of the study and selection of potential sites.

Preparation of Clinical Study Set-up activities.

Clinical Monitoring Visits / Site Management.

Clinical Trial support.

Local or Regional Project Management.

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Regulatory / Importation Services:

Regulatory Processes with  Health Authorities.

Importation Processes of the investigational product and study supplies.
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Elaboration of study documentation Services:
Protocol  Review
Informed Consent Form.
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Training Services:
Training on GCP/ICH for study teams:
Study Coordinators
Clinical Monitor
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Translation Service

Translation of study documentation: English-Spanish / Spanish –English

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Study  Coordinator Services:

Site Study Coordinator Service Unit provides your site with a Study Coordinator, who works closely with the investigator on site to support the protocol procedure activities.

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