Best Quality Research’s Clinical Trials division offers a comprehensive solution for your clinical endpoint study needs. By combining our complete range of Clinical Trial Management services with our highly trained staff of Clinical Research Associates we can offer our clients a "design through report" solution, including, site identification, regulatory compliance, study monitoring, quality assurance, data management, statistical analysis and report writing.

Overview of Clinical Trials

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, if ever.

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Volunteering for a Clinical Trial

When considering volunteering for a clinical trial, it is important to make an informed decision. Below are answers to frequently asked questions that many potential volunteers have about participating in a study.

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Understanding Informed Consent

Millions of volunteers participate in government- and industry-sponsored clinical trials each year. Prior to agreeing to participate, every volunteer has the right to know and understand what will happen during a clinical trial.

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Inclusion and Exclusion Criteria

Understanding Inclusion and exclusion criteria help researchers at Best Quality Research find the most suitable candidates to participate in clinical trials in Florida.

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