THIS IS WHAT WE DO
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Clinical trials are conducted to collect data regarding the safety and efficacy of new drug and device development. There are several steps and stages of approval in the clinical trials process before a drug or device can be sold in the consumer market.
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Drug and device testing begins with extensive laboratory research that can involve years of experiments in animals and human cells. If the initial laboratory research is successful, researchers send the data to the Food and Drug Administration (FDA) for approval to continue research and testing in humans.
Amanda Vega
Site director
OUR TEAM
We strive to bring you the best in research. We gaurantee results you can trust!
Rigoberto Cordero
Founder
Leonardo Garcia
Site Director
GET TO KNOW US
Clinical trial site staff work within and are supported by health service organisations and trial sites to deliver high-quality clinical trials in a safe environment. Clinicians working on clinical trials are responsible for their own professional practice as required by their professional codes of conduct.
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Clinical trial site staff communicate and work with their governing body, clinical and non-clinical managers, clinicians, patients, consumers, and sponsors to conduct clinical trials within their organisation.