INDUSTRY

In the CICA we have a multidisciplinary team with expertise in organizing and conducting clinical trials on drugs (Phases II, III and IV) and medical devices (Class I and II) who will provide personalized support and whose primary objective will be to successfully complete their clinical research. The CICA offers the following services: .

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Quality Managment System

for Conducting Studies

CICA is certified in ISO 9001: 2015, which ensures that all our studies are conducted under strict quality controls in each of its stages

Start up Process

The CICA has personnel responsible for the entire process of beginning the study: Feasibility, Submission to Committees, Submissions to Regulatory Authorities, achieving record times in the approvals of the study

Patient Recruitment

We have personnel dedicated exclusively to the recruitment of patients, who through various tools achieve the total fulfillment of the goals of recruitment and even exceed them

Other Services

In CICA we also provide the following services:

Training for researchers and coordinators

Consulting in Clinical Research

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Study organizations

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Design documentation for Clinical Research

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Imports y Exports

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Development of Standard Operating Procedures

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Pharmacovigilance y Technovigilance

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QUALITY POLICY

In the Centro de Investigación Clínica Acelerada, S.C. we are convenced that the focus in quality is the essence to maintain customer satisfaction, for this is involvement of CICA, SC ensure and maintain high standards of quality in the organization and conduction of all our clinical trials, through a professional teamwork, strict adherence to Good Clinical Practice, managing a quality system at all levels and the continous improvement of its processes.

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