Biotrial, founded in France in 1989, brings over 30 years of experience in conducting clinical trials for pharmaceutical and biotech clients worldwide. About a decade ago, Biotrial expanded its operations to Canada and the United States.
Since 2017, Biotrial Inc. has been conducting clinical trials for global companies and startups in Newark, NJ, near New York City. Biotrial primarily conducts phase 1 clinical trials with healthy volunteers but also recruits patients for its studies.
The Biotrial Medical Research Center in Newark, NJ, is a state-of-the-art, high-tech, and secure facility, conveniently located near cities in the Tri-State area.
Biotrial values work ethic, safety, and transparency. We comply with strict health and ethical standards, adhering to theglobal “Good Clinical Practice” (GCP) standard.
Our top priority is the safety and comfort of our volunteers. Our team is dedicated to providing paid volunteers with the highest quality medical services.
Biotrial, a research medical center for Phase 1 clinical trials
Clinical trials for new drugs are divided into three phases. A phase 1 clinical trial tests the safety and tolerability of a new treatment (side effects, best dose, and timing) on healthy humans. Biotrial Inc. currently carries mainly Phase 1 clinical trials. Our clinical research institute also tests innovative medical devices such as connected T-shirts, helmets, etc.
Strictly supervised clinical trials
In the United States, the Federal government has set stringent regulations and guidelines for clinical research. The US Food and Drug Administration (FDA) is the authority that regulates clinical investigations of medical products.
The FDA works to protect participants in clinical trials and ensure that people have reliable information before deciding whether to join a clinical trial. The studies protocols are approved by the FDA and by the US Ethics Committee, also called IRB for Institutional Review Board.
Main requirements to undertake a clinical trial in humans
- The Food and Drug Administration gives authorization to conduct to a clinical trial in humans only if laboratory tests and studies in animals have shown favorable results.
- Clinical research trials must first be approved by an institutional review board (IRB). An IRB is a committee that has been formally designated to review and monitor biomedical research involving human subjects.
Your safety comes first
At Biotrial, volunteers’ safety is our first priority.
Our volunteers benefit from medical examinations before, during and after any clinical study. Our principal investigators always carefully follow the studies protocols.
To ensure the safety of the participants of our clinical trials, we don’t allow them to enroll in more than a clinical trial. Participating simultaneously in several trials can put a volunteer at serious risk because of the unknown interaction between drugs. It could also seriously hamper the integrity of clinical trials. To avoid these risks, Biotrial uses fingerprint verification at the start of the screening visit.
Transparency is key
We ensure full transparency to our volunteers. We are committed to providing accurate and precise medical information from the screening visit throughout the trial.
Your privacy is protected
Our volunteers’ privacy is protected by the Health Insurance Portability and Accountability Act of 1966 (HIPAA). This Law requires that individual participants’ information, including medical information, remains confidential.
What makes a good Research Medical Center?
- We put our volunteers' satisfaction first
- Our staff has excellent interpersonal skills
- We invest in our infrastructure
- We work as one
We are one of the most trusted medical center for clinical research in the US East Coast.
We count on you to help us provide the most advanced remedies for future generations.
