ABOUT ACTIVA8®


ACTIVA8­­­® is a service company for contract research organization and consulting in the management and development of Clinical Trials in Latin America.

ACTIVA8­­­® is created from the direct demand of the pharmaceutical industry and biotechnology companies with the purpose of filling the need for managing clinical research of drug development, medical devices and diagnostic test studies.

Why to work with ACTIVA8® :

Partnership :

We offer you our flexibility, as we accommodate to your priorities, schedule and calendar whenever it is needed. ACTIVA8­­­® personnel work side by side with you and become  effective partners in your project development

Quality:

ACTIVA8­­­® works under ICH , (International Conference on Harmonization) guidelines /GCP (Good Clinical Practices) compliance quality.
ACTIVA8­­­® has its own standard operating procedures (SOP's)  for all clinical operations. We can also work under your own company's SOP's, according to your requirements and needs.

ACTIVA8­­­® works under specific ISO for medical device research and has specific SOP's  for medical device studies.

ACTIVA8­­­® personnel receive constant updated training in clinical trial procedures.

Experience and Knowledge:

We have in-depth knowledge of the Latin American region's regulatory processes and management for local and global clinical trials.
ACTIVA8­­­® has alliances with expert clinical research professionals across the Latin American region to help you with your clinical trials.
ACTIVA8 has alliances with expertise clinical research professionals across the Latinamerican Region to help you with your clinical trials.


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