Clinical Trials

Participants Privacy And Rights

Participants Privacy And Rights

Volunteer Eligibility

To ensure the safety of subjects who volunteer for clinical trials as well as preserving the integrity and credibility of the data reported, all studies are conducted under regulatory compliance and strict protocol adherence.

The rigorous methodology of executing a clinical trial, most significantly through the controlled and random intervention of human volunteers by the investigator, makes this epidemiologic study design one of the most powerful approaches to demonstrating causal associations in the practice of evidence-based medicine.

We respect the participant’s privacy and rights .We run the trial for our sponsors to plausibly achieve the intended goals of the study through enrollment and allocation techniques, selected endpoints, methods of comparison.

Emphasis on patient safety is our priority. We run phase 2 and phase 3 trials.

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